Y-DNA & the Griffis Paternal Line Part Five: Using Y-DNA & Locating a Griff(is)(es)(ith) Relative and Other Leads

You can only go so far with Y-DNA test results. As stated in prior parts of this story, the ability to combine information from a wide variety of sources will ultimately lead to validated results, promising leads and stories. Oftentimes, in my limited experience I find that many individuals who have completed Y-DNA tests do not do much once they get the results. This is perhaps due to their unrealistic expectations of what the tests will provide. Or given the nature of the field, DNA testers do not know what to do with the results. I have found getting the test results is just the start of the process. They point you in a certain direction. The next steps are then in your hands in terms of trying to make sense of the results. 

I can attest that I have not pushed the envelope in terms of analyzing Y-DNA results as much as possible. It takes a fair amount of time, energy and imagination. It also requires the ability to learn and understand how to interpret the results and use various mathmetical tools to analyze genetic data. DNA companies such as Family Tree DNA (FTDNA) provide access to a wealth of data, some of which is analyzed and packaged in innovative ways. FTDNA also provides working groups to assist in locating genetic matches and providing forums for assistance. However, there are other instances where one is on their own and required to personally gather FTDNA results from fellow testers in order to create “genetic trees” or uncover genealogical discoveries.

G-Haplogroup is a Modern Day Y-DNA Genetic Minority Group

In addition to the challenges of grappling with analyzing genetic data, despite the explosive growth of DNA testing, there is a dearth of data for testers of certain Y-DNA haplogroups. The Griff(is)(es)(ith) patrilineal line is part of the G-haplogroup. The G-haplogroup is a modern day genetic minority group at least in terms of potential testers and actual test kits in the FTDNA database.

The testing of Neolithic remains in various parts of Europe has confirmed that a major sub-branch of G, haplogroup G2a, was one of the dominant lineages of Neolithic farmers and herders who migrated from Anatolia to Europe between 9,000 and 6,000 years ago. They were part of a second massive wave of humans to migrate into Europe. However a third wave, coming from the Steppes, brought an additional Y-DNA genetic mix and eventually overtook the dominance of the G-haplogroup genetic presence. This third wave was predominately composed of the Y-DNA R-Haplogroup. [1]

By the Iron Age, the G2a subclade population in most of Europe had been genetically replaced as one of the predominate genetic paternal lines by the Indo-European migration of the R-Haplogroup. This was also followed by Celtic warfare in northwest Europe.. The net result was the diminished presence of G haplogroup men in Europe.

The ‘third wave’ of migration patterns into Western Europe belonged primarily to haplogroup R1b-U152. But as with any large scale migration pattern, the historic waves of migratory patterns often contain a mixture of genetic groups. Going back to our discussion in part two of this story about the differences between cultural and genetic genealogy, the macroscopic movements of genetic groups are logically separate and invisible from the cultural trappings of the actual migratory human groups. It appears that this third wave also carried a substantial minority of G2a-L140 lineages (of which the Griff(is)(es)(ith) line is part of) along their migration route. The net result of all of this is the G-haplogroup descendants in modern day Europe are a minority Haplogroup.

G2a makes up 5 to 10% of the population of Mediterranean Europe, but is relatively rare in northern Europe. The only regions where haplogroup G2 exceeds 10% of the population in Europe are in Cantabria in northern Spain, in northern Portugal, in central and southern Italy (especially in the Apennines), in Sardinia, in northern Greece (Thessaly), in Crete, and among the Gagauzes of Moldova – all mountainous and relatively isolated regions. Other regions with frequencies approaching the 10% include Asturias in northern Spain, Auvergne in central France, Switzerland, Sicily, the Aegean Islands, and Cyprus.

“. . . (T)he frequency of haplogroup G decreases with the distance from the boundaries of the empire. Haplogroup G is much rarer in Nordic and Baltic countries nowadays than in Great Britain, despite the fact that agriculture reached those regions around the same time. It is therefore not inconceivable that a part of the G2a in Great Britain, and especially in Wales (where G2a is the highest) should be of Roman origin. “ [2]

Illustration One: Distribution Map of Haplogroup G2a-L497 in Contemporary Europe

Source: Maciamo Hay, Haplogroup G2a, Eudepia [2] | Click for Larger View

This means, by inference, there is a smaller pool of available males in Europe to obtain Y-DNA comparative test results. This is reflected in the current distribution of Y-DNA tests results maintained by FTDNA. [3] Test results associated haplogroups of testers residing in in modern Europe and the United States have increased dramatically (for example Haplogroups R, J, and I).

Illustration Two provides a time tree view of the FamilyTreeDNA Haplotree, showing branch lengths in thousands of years. The timeline is oldest (left) to more recent (right). Numbers adjacent to each clade are counts of downstream branches a given haplogroup.. Younger branches are collapsed for readability: 5,000 years ago is depicted in the main tree. 2,000 years ago is depicted in the much larger Haplogroup R tree. While not the smallest Haplogroup in terms of the number of branches documented, the G-Haplogroup is nonetheless smaller than many of the other haplogroups found in Europe. [3]

Illustration Two: Family Tree DNA Haplotree Summary Dec 2020 of the Number of Haplogroup Branches Documented.

Click for Larger View.

Coupled with the present day small population size of G-Haplogroup men in Europe, there are the genetic repercussions of “Brick Wall” challenges that were the result of colonial immigration to the Americas.

The Brick Wall: Colonial Immigration

Many amateur American genealogists lament about the Atlantic Ocean as the ‘brick wall’ in the uncovering ancestors who immigrated to the Colonies. There are historical and social structural parameters that shape and influence the probability of successfully finding descendants through genetic analysis and traditional genealogical research. 

It is inherently easier to document ancestry on the American side of the Atlantic. It is objectively more difficult to discover genetic leads and traditional paper documentation to link our immigrant descendants with European descendants. 

For many Americans, notably those who can trace their last known ancestor to colonial times, the last known connection will be the son of or the original immigrant son from Europe. In our case, it is William Griffis born in 1736 in Huntington, New York.

The original immigrant or the descendant of the original immigrant is in genetic genealogy the founder, a DNA bottleneck who “resets the odometer” on DNA mutations; and descendants start with zero diversity. This is a common pattern with profound effects on mtDNA or Y-DNA research. Bottlenecks on the European side (due to war, natural disaster, disease, etc) can further compound the problem of finding genetic matches 

From an historical demographic and economic perspective, there are fewer descendants to trace back in Europe compared to the United States. Colonial America also had a higher literacy rate and great interest in record keeping which greatly aids efforts in locating documentation associated traditional genealogical research. Families that remained in Europe faced socio-economic hardships that resulted in lower fertility rates, smaller families, and higher mortality rates.  [4]

The life experiences for family member who immigrated to the colonies were substantially different from their respective family members who stayed behind in Europe. While the first 17th century settlers had fearsome mortality rates, poor diets, and their settlements were dependent on the net import of foodstuffs, their life conditions comparatively improved over time and generations compared to their European relatives. 

From a demographic, social, and economic standpoint, individuals who immigrated to the colonies experienced a set of different life experiences. European counterparts in western Europe had smaller families, higher mortality rates, limited economic capabilities and resources, and lived in urban areas. This contrasts with the life experiences of a family member who immigrated to the colonies. Abundant natural resources, higher wages, and cheap land contributed greatly to American colonialists’ standards of living. The period during which Americans most clearly led Britain in purchasing power per capita was in the colonial era.  American colonists also had much more equal incomes than did West Europeans at that time. [5]

It does not seem difficult to find out the reasons why the people multiply faster here than in Europe. As soon as a person is old enough he may marry in these provinces without any fear of poverty. There is such an amount of good land yet uncultivated that a newly married man can, without difficulty, get a spot of ground where he may comfortably subsist with his wife and children. The taxes are very low, and he need not be under any concern on their account. The liberties he enjoys are so great that he considers himself as a prince in his possessions. [6]

The colonies had some of world history’s highest population growth rates, not only in the initial settlement phases, but all the way up to the Revolution. Between 1700 and 1780, population grew at 2.9 per cent per annum for New England and also for the Middle Colonies, and at 2.4 for the Southern colonies. Furthermore, these rates were well above those in the rest of the world. The net fertility in early America was more than double that of Europe. American families from 1650 to 1850 averaged 4.8 children to adulthood.

Two sources of population growth (high fertility rates and higher life expectancy rates) with their opposing implications for the level of income per capita, were at play in the colonial era. The American colonists had extraordinary rates of natural increase, fed by early marriage and high fertility, and by low mortality (outside of the South – excluding the unfortunate effects of slavery). As early as 1751 Benjamin Franklin attributed all of these features to the abundance of land, and half a century later Robert Malthus agreed. [7]

A 1650 emigrant will have 200-fold more descendants than a sibling who stayed in Europe. This, plus DNA testing bias, is why an American DNA tester will seldom find a European connection. [8]

Illustration Three: Example of Two Brothers’ Descendants

Source: Rob Spencer [6] | Click for Larger View

The explosive growth of DNA testing in the United States and Americans’ interest in DNA testing has led to a current situation where DNA databases are heavily slanted to American stories. That explosion coupled with the historical, socio-economic, and demographic patterns on each of the Atlantic during colonial times leads to large scale patterns that have essentially created a steep uphill path for individuals in the United State finding colonial descendants in Europe..

The Griff(is)(es)(ith) family that started from William Griffis certainly fits this argument about tracing colonial immigrant families and their subsequent growth in the new world. William had 12 children, ten of which were males: a good start for the continuation of the Y-DNA line. There are over 1,100 descendants (including family members by marriage) of William Griffis between his life and present day.

The following Illustration Four depicts a visual depiction of the founder effect for the Griff(is)(es)(ith) family through a novel rendering of a family tree. [9] The top of the tree is William Griffis. In addition to the various branches in the family tree, it also illustrates the number of descendant lines of extinction for various generations (the ‘fanning’ of branches in the tree diminishes) as well as the diminishing size of families through time (the width of th ‘fans’ of branches). The visualization also portrays the age longevity of individuals in the tree.

Illustration Four: Descendants of William Griffis – 1773 to the Present

Being part of a present day minority haplogroup, facing the challenges associated with the genetic brick wall of colonial immigration, and the American bias of Y-DNA testing certainly does not raise the expectations of finding Y-DNA genetic discoveries in Europe, regardless of the advancements made in DNA testing.

As will become evident as the story unfolds, the results are not entirely earth shattering but there are surprises nonetheless.

Review of Y-DNA Results

Based on the results of my Big Y 700 test from Family Tree DNA (FTDNA), I was able to compare similar test results from other males who completed the Y- 12, Y- 25, Y-37, Y-67, Y-111 or Big Y 700 Y-DNA tests. Short tandem repeats (STR) matches are limited to results for only the 111 identified STRs. The STRs beyond the 111 are used for predicting a more refined assignment of a Haplogroup or documenting a new branch in the haplotree.

I originally started my examination of potential Y-DNA STR matches with the Y-37 and Y- 67 test results. The more STRs used for comparison will provide more reliable results. It is like comparing two digital photographs of the same subject but one has more pixels and the other. The photograph with more pixels will provide more detail. Without additional traditional genealogical information or knowledge of surnames, using the results from the Y-111 test is the most reliable strategy for analyzing STR results. However, if another Y-DNA tester had taken a test with fewer STRs and had a similar surname or self reported common ancestor, then it is prudent to compare their Y-DNA results. This became apparent as I progressed with my research.

As indicated in earlier parts of this story, my Big Y 700 Y-DNa test confirmed my affiliation with the G haplogroup and documented that the Griff(is)(es)(ith) patrilineal line was also part of the L-497 subbranch of the haplogroup. Reviewing their work was a good start for my research.

The overwhelming majority of northern and western Europeans who belong to the G2a subclade fall specifically within G2a-L140 subclade. [10] The following ‘breadcrumb’ line traces back from my terminal SNP haplogroup:

G-L140 > G-PF3346 > G-PF3345 > G-L497 > CTS9737 > Z1817 > Z727 > FGC477 > Z6748 > Y38335 > Z40857 > Y132505 > BY211678.

Illustration Five provides a graphic view of the breadcrumb line of haplotree branches to my terminal point on the G-haplotree. It also indicates the approximate date when the MRCA of the branch was born. My strategy for looking for possibleY-DNA matches among the Y-DNA test kits, involved going down the breadcrumb branches of the haplotree to a branch that was created closer to the present. The G-40857 branch started around the time of the Norman invasion of the British Isles 91000 CE). It made sense to start there for possible matches.

Illustration Five: SNP Breadcrumbs to My Terminal SNP

Click or Larger View.

From the L-497 branch (which represented the initial stages of the second wave of modern human migration into Europe) I could narrow my search by going down the haplotree branches. Moving through ‘genetic history’ and following the westward migration of the haplogroup in Europe to the most recent branch: G-BY211678. The most common recent ancestor (tMRCA) for this branch was estimated to have been born around 1500 CE. This would represent a “recent” group of descendants that conceivably had descendants in a geographic area where William Griffis had descendants.

Based on the current population of FTDNA testers who completed one of the six types of Y-DNA tests, eleven individuals that were members of the L-497 project were the closest genetic matches within my haplotype. Table One, which has been mentioned in the prior story, provides the STR results of arranging test kits based on haplogroup affiliation. Twelve test kits (including mine) were grouped in the G-BY211678 haplogroup.

For genealogy within the most recent fifteen generations, STR markers help define paternal lineages. Y-DNA STR markers change (mutate) often enough that most men who share the same STR results also share a recent paternal lineage. Table One displays Y-Chromosome DNA (Y-DNA) STR results for individuals that either tested or were predicted positive for Y132505+ and BY211678+ for the SNPs associated with these haplogroups.

The table uses a colorized format to display the results. [11] The columns display each project member’s kit number, paternal ancestry information according to project settings, the paternal tree branch (haplogroup), and actual STR marker results (up to 111 markers in this table). In the haplogroups column, haplogroups in green are confirmed by SNP testing. Haplogroups in red are predicted. Above each subgroup, the table displays the minimum, maximum and mode values for each STR marker in the subgroup. STR marker values that differ from the mode values are color-coded.

Table One: Haplogroup G-L497 Y-DNA Project – Y-DNA Colorized Chart

Source: FTDNA L-497 Work Group DNA Results | Click for larger view

Using various FTDNA based analytical tools and other novel applications from amateur genealogists, eight of the eleven test kits were found to be ‘relatively’ close as genetic Y-DNA matches.

Table Two provides information on ‘how close’ the eight test kits are in terms of genetic distance. All but one of the test kits are associated with individuals in the United States. Kit number 149885, the surname of the tester is Gough, is from England. Two of. the eight are ‘two genetic steps’ from me while the remaining six tests kits are four genetic steps. The number of steps from our respective MCRA are not necessarily the same. As stated in the prior story, the number of STRs compared has an impact on how to interpret genetic steps.

Although the test kit 125476, whose tester’s last name is Griffith (first row of the table), only tested for the Y-37 test, his test results are 2 ‘genetic steps’ different from my test results. This means, based on a Y-37 test comparison, Mr. Griffith and I share a common ancestor around 8 generations ago or ‘give or take’ between 2 to 20 generations..

Based on a Genetic Distance of 2 at the Y-37 test level, I and Henry Vieth Griffith are estimated to share a common paternal line ancestor who was, with a 95% probability, born between 1250  and 1850 CE. The most likely year is rounded to 1650 CE. This date is an estimate based on genetic information only. Eight generations would be around the revolutionary war period in America and around the time that William Griffis was born! [13]

Table Two: STR Haplotype Matches with James Griffis Based Minimally on Y-37 Test

Kit
No.
Surname
of Tester
STR 
Markers 
Tested
Genetic
Distance
(GD)
Likely
Common
Ancestor
(Genera-
tons)
MRCA
Based 
on GD
[12]
Earlest
Known 
Ancester
125476Griffith372 Steps8 (2-20)1650 CEWilliam
Griffis
39633Compton372 Steps8 (2-20)1650 CEUnknown
154471Williams1114 Steps3(7-15)1700 CEWilliam
Williams
285488Williams700**4 Steps3(7-15)1700 EGeorge
Williams
294448Williams1114 Steps3(7-15)1700 CEGeorge
Williams
285458Williams1114 Steps3(7-15)1700 CEGeorge
Williams
36706Williams674 Steps11(4-22)1500 CEWilliam
Williams
149885Gough374 Steps14(6-28)1300 CEGough
** For Y-700 testers, the Y-111 markers are used for matching purposes.
Source: FTDNA myFTDNA Y-DNA Match Results for James Griffis

The following provides an explanation of the information found in Table Two

Surname is the actual surname of the tester.

Markers Tested indicates the total number of STR markers tested. Only markers from those tests were used for the match. 

Genetic Distance (GD) refers to the number of mutational differences in tested STRs between my results and the individual tester. Fewer differences can indicate a closer relationship to a shared paternal line ancestor. This is used to rank order possible genetic matches among Y-DNA test kits. [12]

Common Ancestor refers to the estimated number of past generations that I and the tester possibly share a common ancestor based on a 90+ percent confidence interval. Since each STR marker has a different mutation rate, identical Genetic Distances will not necessarily yield the same probabilities. Someone else with the same Genetic Distance may have different probabilities, because the distance was prompted by mutations in different markers, with different mutation rates. The numbers in the parentheses represent the confidence level range of generations.

MRCA is based on an estimate time when the common ancestor was born.

Earliest Known Ancestor is self reported by the owner of the test kit.


Another Y-DNA tester is purportedly 2 genetic steps from me as well. The surname associated with the test kit is “Compton” and no earliest known ancestor was reported with the test results. I have not found any relatives through tradition genealogical research with the surname of Compton.

Given the nature of the late adoption of surnames among the Welsh, being related to this gentleman is not necessarily ruled out. While it has been stated that one should expect the presence of surnames for tMRCA’s with branches that are less than 25 – 30 generations ago, I am assuming that range is more like 20-25 generations ago for Welsh surnames. [14] The statistical deviation of 2 genetic generations based on a Y-37 STR test is relatively wide. Similar to my test result comparison with Henry Griffith, based on a Genetic Distance of 2 at the Y-37 test level, I and Mr. Clinton K Compton are estimated to share a common paternal line ancestor who was, with a 95% probability, born between 1250 and 1850 CE. The most likely year is rounded to 1650 CE.

The remaining six testers listed in Table Two are four genetic steps different from my test results. One of the test kits is based on Y-37 results, one on Y-67 results, three on Y111 results and one on the Big Y 700 test kit result.

What is interesting among these six test kits, the common surname is Williams. While I do have any traditional genealogical documentation which connects the Griffis family with other individuals with the Williams surname, perhaps 15 to 22 generations back there might be a common ancestor with the Williams surname.

Illustration Six: Emergence of Surnames in Genealogical Research Depicted in a Genealological Dendrogram

As discussed in earlier stories, the use of surnames in Wales was not widespread until the sixteenth and seventeenth centuries. In the greater part of Wales, the ancient patronymic naming system continued: having children identified in relation to their father. This meant that surnames in the 1600’s and and 1700’s did not take on the weight of significance that they have for present generations. Using a surname was similar to using a first name, they changed based on what was conferred by prior generations and also what one wanted to use as a surname.  There was a wide time variation when surnames were adopted in various parts of Wales. Surnames became the norm by 1750 across the coastal plain of south Wales and along the eastern border with England. [15]

The ten most common surnames in Wales in 1856 were Jones (13.84%), Williams (8.91%), Davies (7.09%), Thomas (5.70%), Evans (5.46%), Roberts (3.69%), Hughes (2.98%), Lewis (2.97%), Morgan (2.63%) and Griffiths (2.58%). [16]

The STR Results Using Dendrograms

I used the FTDNA data from the L-497 project as data input into Rob Spencer’s Y STR Clustering and Dendrogram Drawing program [17] and filtered the data to only include test kits within the G-BY211678 haplotree branch (re: Illustration Six above). The dendrogram provides a sense of genetic distance between the test kits and approximate generations from the most recent common ancestors.

The dendrogram provides a genetic tree diagram of test kits that are listed as rows in the dendrogram. The nodes to the branches in the tree represent a most recent common ancestor. Time, as measured in the number of generations from the present, starts from the right and proceeds to the left. The haplogroup for each test kit is listed. Some of the haplogroups associated with test kits are very basic or reflect major ‘trunk branches’ in the G-haplotree. This is due to the type of Y-STR test that was used for a particular kit. If someone completed a Y-37 test, given the limited number of STR markers tested, haplogroup prediction would also be limited. The paternal ancestor, reported by the tester, is also listed in the dendrogram.

Illustration Six: Y-STR Dendrogram of FTDNA Test Kits in the G-BY211678 Haplogroup

Click for larger view

The genetic relationships between the test kits are fairly apparent. What is evident is the close genetic distance between Mr. Griffith and my test kits. His test kit is listed as G-M201 “William Griffis b.c. 1733, Huntington, NY and my test kit is listed as G-BY211678 “William Griffis b. 1736”. Consistent with the FTDNA’s  results from FTDNATiP™ genetic steps analysis, my test kit and Mr. Griffith’s test kit suggest we share a common ancestor approximately 8 generations ago who was born in the mid 1600’s to early 1700’s.

The dendrogram also suggests that a common ancestor is shared with eight test kits that identify their respective paternal ancestors as having the Williams and Gough surnames. Our most recent common ancestor may have been born about 14 generations ago. Using 33 years for a generation [18], this would be around 1560 CE. The approximate date of our MRCA is prior to the time when surnames were prevalent in Wales.

STR Results Portrayed in a Phylogenetic Tree

I also used the FTDNA data from the L-497 project as data input into Dave Vance’s SAPP program to develop a phylogenetic tree that graphically outlined the genetic distance between the test kits within the haplogroup. The program is relatively easy to use and graphically provides an intuitive approach to visualize the possible genetic relationships between various DNA test results. The program is referred to as the SAPP analysis (Still Another Phylogeny Program). The current version that was used in my analysis was SAPP Tree Generator V4.25. [19]

The resultant phylogenetic tree created nodes that represent tMRCA based on key differences between specific STR markers based on the allele values for the respective STR markers. Basically the program creates a genetic tree of test kits based on the comparison of differences between the allele values for the STR markers. It transforms the information in Table One into a tree.

The following phylogenetic tree in Illustration Seven was created (click on the image of the thumbnail of the tree to be able to actually see the table) or see the PDF file – you can increase the size of the PDF file to better viewing.

Illustration Seven: Phylogenetic Tree Results for FTDNA STR Test Results for Individuals within the G-BY211678 Haplogroup (Click for Larger View)

Click for Larger View. | PDF file version

The analysis of STR differences between the 12 test kits resulted in a  phylogenic tree with three major nodes. The most recent common ancestor that started the G-Y132505 haplogroup branch is estimated to have been born around 1250 CE and the birth date of tMRCA for the subsequent G-BY211678 haplogroup is 1500 CE. It is estimated the MRCA for all of the 12 test kits is 23 generations or 1300 CE.

There are three major nodes in the phylogenetic tree. Descending from the MCRA, three individual test kits are listed directly from the MCRA. One of the three major nodes, Node #13, lists descendants of William Griffis.  Node #13 is based on key STR  differences in five STR markers: DYS456, DYS570, CDYa, DYS617 and DYS 715. Both my kit and Henry Griffith’s test kits are part of this node. Another major node, Node #16, groups test kits that have a paternal ancestor listed as William Walmsley and William Williams. Another major node, Node #18, lists test kits that had more recent STR mutations (an estimated TMRCA of 3 generations – around 1800 CE). The  test kit with the paternal ancestor named Gough is listed directly off the major node.

The Results: The Big Picture

In general, while the results from analyzing STR Y-DNA data are sparce, the analysis underscored the value of genetic genealogical analysis for unearthing discoveries associated with each of the three periods of genealogy, particularly for potential lineages and genealogies. [20]

Illustration Eight: The Three Periods of Genealology

Finding genealogical matches are slim. The size of the current database of Y-DNA testers within my specific G-haplogroup is relatively small. The probability of finding matches is obviously related to the size of the population that has completed a Y-DNA test with the particular company that you are utilizing. While DNA testing has appreciably increased over the past 10 years, Y-DNA testing has specifically increased at a lower rate than the popular ‘ethnic heritage’ tests. Like fly fishing, I knew my ability to snag a ‘lead’ through Y-DNA analysis might be slim but a catch is always delightful.

It came as no surprise that the available test results for comparison for potential genetic matches are presently small. There were only a dozen or so test kits for comparison in one of the FTDNA working projects. There may be additional test kits to compare but it involves a more active search on my part to search the FTDNA complete database.

Matches with different surnames were found in the lineages period of genealogy.  Since the Griff(is)(es)(ith) surname is purportedly a Welsh surname, the use of surnames did not become firmly established in certain parts of Wales until the late 1700’s to mid 1800’s. Based on my traditional genealogical research I knew the Griffis family line had three spellings of the surname (Griffis, Griffith, and Griffes) in America. Y-DNA tests have corroborated that finding genetically related ancestors with different surnames in Europe is evident. The next step is to see if any of the Williams clan are part of our genetic lineage.

Finding genealogical matches currently confirmed through traditional research. The Y-DNA test did indeed find a match with an individual that I have already documented in my family tree. I might be able to find additional clues to male family members that are descendants of William Griffis in the future.

Finding genealogical matches that point to Wales.  It appears Y-DNA test results point to ancestors in the area we currently call ‘Wales”. Obviously, one’s ancestors could be Welsh and have lived in London or other parts of the British Isles. This is investigated in the next story.

Identify unknown ancestors and lineages in timelines where no records exist.  The Y-DNA test results have narrowed the search of male ancestors of the Griff(is)(es)(ith) paternal line to specific genetic Y-DNA lines in the G-haplogroup in the British Isles.

Identify ancient groups and migration patterns associated with the genetic paternal line. I certainly have obtained information about ‘deep ancestry’. Viewing the patrilineal line at a higher, macroscopic anthropological level provides a novel perceptive on the origins of the lineage. More on that in subsequent stories.

Further research into the possible background of the remaining test kits may produce worthwhile results! WHO KNOWS, we might be related to a few Williams and a Gough and a Compton a few centuries ago!

Corroboration of a Family Tie: Henry Vieth Griffith

The results of the Y-DNA testing thus far have confirmed one distant Griffith relative: Henry Vieth Griffith.

Henry Vieth Griffith and Arvilla Rogers
Dave Sickler originally shared this  photograph on an ancestry.com family tree on 13 Jan 2021

Henry Vieth Griffith was originally discovered through traditional research. Y-DNA analysis confirmed the results of traditional genealogical research. Through the course of researching various on-line family trees, coupled with access to personal family histories surrounding the descendants of James Griffis, William Griffis’ second son, I was able to document Henry Griffith’s family ties.

In the course of conducting my on-line research prior to completing Y-DNA tests, I discovered a defunct website “Gruffydd Genealogies: Griffi(th)(n)(s)(ng)Surname DNA Project“.

The website had a link entitled “Pedigrees” which listed family trees with Kit Numbers, brief information on the paternal ancestor and email contacts. At that time I had no idea what a ‘Kit Number’ was nor was it immediately apparent that the website represented the results managed by FTDNA. [21]

On a Pedigree link on the website it listed a number of Family Pedigrees found in this Y-DNA surname research project. One of the pedigree’s got my attention: “ #49, Kit Number 125476, William Griffith, born 1773 of New York, married Abiah Gates ” and provided a contact email address”.

“Eureka! I found a relative! “

Unfortunately, my repeated attempts to send emails provided no responses. The email address appeared to be a dead-end. Moreover, the link to the family tree for this Kit number returned with a ‘404’ web error, meaning the link no longer linked to an existing web page. I did not realize until later on in my research that the email address on the website was Henry’s wife’s email address. Sadly, Arvilla Griffith passed away in 2014.

While the website was no longer being actively managed, I did not realize that the website was the early precursor of the current FTDNA Griffi(th)(n)(s)(ng) Surname project of which I am now a member. The project administrator listed on the website is no longer involved with the project but some of the links on the old site still direct the reader to current information on DNA results for another current FTDNA project: the L-497 haplogroup project!

At the time of this discovery of the defunct website, it merely provided, for my research, another confirmation that “William Griffith(is)” married Abiah Gates.

Through my continued research of genealogy material posted on various family trees, I found a number of sources that ultimately provided bits and pieces of the James Griffis (b. 1758) family line of descendants – sufficient information to progressively put puzzle pieces together to develop ties between Henry Vieth Griffith and the descendants of William Griffis.

All said and done, tracing Henry’s line of descent up to William Griffis and back down the tree to me indicates that Henry is my 5th cousin once removed.

Illustration Eight: Most Recent Common Ancestor for Henry Griffith and James Griffis

Henry Vieth Griffith, was a descendent of James Griffis, William’s second son. Here is Henry’s surname line:  

  • William Griffis, born 1736 Huntington ,NY;
  • James William Griffis, born 04 June 1758 Suffolk, Co, NY, died 21 November 1838, Suffolk, County, NY;
  • James Harvey Griffith, born 19 August 1801 Huntington, NY, died 11 April 1883 Rockaway, Queens NY; 
  • James Harvey Griffith, born 23 April 1854, died 26 Sep 1918 Barrington, Bristol, Rhode Island;
  • Benjamin Fessenden Griffith, born 8 March 1897 East Rockaway Nassau NY, died 27 May 1977 Suffolk County, NY; and
  • Henry Vieth Griffith (17 October 1923 Barrington RI – 20 May 2017 Weslaco, TX) 

It is interesting to note that James Griffis’ descendants reverted to the Griffith spelling of the surname. With one exception, all the descendants of James Griffis spelled their surname as ‘Griffith‘. the reason for the reversion to the Griffith spelling is not known. One of the daughters, Abiah, possibly spelled her maiden name as Griffis or Griffiths. [22] Many of his descendants continue to live in Long Island and New England area. 

James Griffis and Sarah Totten had seven children. All of his children were baptized under the name of Griffith and other records associated with his children indicate the use of Griffith as a last name. It is interesting to note that church records indicate that the first six children were baptized in a group ceremony on the same day on August 4 in 1797. [23]

Table Three: Children of James William Griffis

Second Generation of
Griffis Family
Third Generation
James William Griffis
1758 – 1838
Suffolk Co. NY
Jerusha Griffith (female)
1785 – 1859
Suffolk Co. NY
Abiah Griffis (female)
1786 – 1871
Suffolk Co., NY
Sarah Griffith (female)
1787 – 1847
Suffolk Co, NY
Jesse Griffith (male) 
1788 – 1855
Suffolk Co., NY
William Griffith (male)
1791 – 1879
Suffolk Co., NY
Peter Griffith (male)
1796 – 1874
Suffolk Co., NY
James Harvey Griffith (male)
1801 – 1883
Suffolk Co., NY

For about 8 generations, there were 53 male descendants of James Griffis. All used the ‘Griffith’ surname. Thirty-seven of the descendants lived in the counties contiguous to or part of the New York City area. Eight lived in Connecticut and four lived in Rhode Island. One descendant lived in Rensselaer county, NY and one lived in Union county, NJ. Four lived in Jefferson county, KY; one is Hidalgo county, TX, Chester County, PA, and Broomfield county, CO.

I have not looked closely at the range of geographical mobility for each of the male descendants. The geographic mobility for most of descendants was limited within the area noted in the table and maps. Henry Vieth Griffith was one notable descendant living outside of the New England area. Military life took him to many places and he appears to have had the most extensive mobility of his descendants over his lifetime.

Illustration Nine: Locations of Descendants of James Griffis in New York State

Click for Larger View

Illustration Ten: Locations of Descendants of James Griffis in Connecticut and Rhode Island

Descendants of James Griffis residing in Connecticut, click for larger view.
Descendants of James Griffis residing in Rhode Island, click for larger view.

Henry Vieth Griffith’s father, Benjamin Fessenden Griffith, lived in Rhode Island where Henry and his siblings were born. When Henry Vieth Griffith was born on October 17, 1923, in Barrington, Rhode Island, his father, Benjamin, was 26 and his mother, Sara, was 26.

The following is an undated newspaper article about Henry and one of his brothers, Harvey K. Griffith, when they both were in military service during World War II.

Illustration Eleven: Newspaper Article About the Two Griffith Brothers

Click for Larger View

Henry and Arvilla met in Oklahoma City, OK during World War II. They were married on August 17, 1944, in Oklahoma City, Oklahoma. They had a long and event filled life together. Shortly before Arvilla’s death in 2014, they celebrated their 70th wedding anniversary. 

They both were in military service during World War II. Henry made a career out of his military service to the country. While rising their family and following her husband around the world in his military career, Arvilla earned credits at 11 different universities, received her Bachelor’s degree and then went on to obtain her Doctorate in Education. They had five children during their marriage. Their retirement years were spent in southern Texas, Henry passed away on May 20, 2017, in Weslaco, Texas, at the age of 93, and was buried along with Arvilla, in Fort Sam Houston National Cemetery, San Antonio, TX. [24]

Henry or Arvilla or both were evidently were interested in genealogy. This was reflected in Henry completing a Y-DNA test. I only wish I was able to have met Henry and Arvilla before they passed away.

Illustration Twelve: Headstones for Henry Vieth Griffith and Arvilla Rogers Griffith

Sources

The Featured Image at the top of the story is a section of a spreadsheet of Y-DNA test kit results managed by the Haplogroup G-L497 Y-DNA Project. Highlighted rows point to my test kit and Henry Vieth Griffith’s test kit. The chart page displays Y-Chromosome DNA (Y-DNA) STR results that are grouped on the baiss of their similarity on SNP haplogroup results. The columns display each project member’s kit number, paternal ancestry information according to project settings, the paternal tree branch (haplogroup), and actual STR marker results. Above each subgroup, the minimum, maximum and mode values for each STR marker in the subgroup are displayed. STR marker values that differ from the mode values are color-coded.

[1] Andrew Curry, The first Europeans weren’t who you might think, National Geographic, Sept 2019, https://www.nationalgeographic.com/culture/article/first-europeans-immigrants-genetic-testing-feature?loggedin=true&rnd=1676757061299

Early European Farmers, Wikipedia, This page was last edited on 5 February 2023, https://en.wikipedia.org/wiki/Early_European_Farmers

Reich, David Who We are and how We Got Here: Ancient DNA and the New Science of the Human Past. Oxford University Press. 2018

Lazaridis, Iosif; et al. (July 25, 2016). “Genomic insights into the origin of farming in the ancient Near East”. Nature. Nature Research. 536(7617): 419–424. Bibcode:2016Natur.536..419L. doi:10.1038/nature19310. PMC 5003663. PMID 27459054 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5003663/

González-Fortes, Gloria; et al. (June 19, 2017). “Paleogenomic Evidence for Multi-generational Mixing between Neolithic Farmers and Mesolithic Hunter-Gatherers in the Lower Danube Basin”. Current Biology. Cell Press. 27 (12): 1801–1810. doi:10.1016/j.cub.2017.05.023https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5483232/

Lazaridis, Iosif (December 2018). “The evolutionary history of human populations in Europe”. Current Opinion in Genetics & Development. Elsevier. 53: 21–27. arXiv:1805.01579doi:10.1016/j.gde.2018.06.007https://www.sciencedirect.com/science/article/abs/pii/S0959437X18300583

Shennan, Stephen (2018). The First Farmers of Europe: An Evolutionary Perspective. Cambridge World Archaeology. Cambridge University Press. doi:10.1017/9781108386029. ISBN 9781108422925

Nikitin, Alexey G.; et al. (December 20, 2019). “Interactions between earliest Linearbandkeramik farmers and central European hunter gatherers at the dawn of European Neolithization”Scientific Reports. Nature Research. 9 (19544): 19544. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6925266/

[2] Maciamo Hay, Haplogroup G2a, Eudepia, Last update January 2021, https://www.eupedia.com/europe/Haplogroup_G2a_Y-DNA.shtml

[3] The following graphics illustrate the smaller sample size of Y-DNA test data for the G Haplogroup managed by Family Tree DNA (FTDNA), source: 2020 Review Of Big Y, FTDNA Blog, Feb 1, 2021, https://blog.familytreedna.com/2020-review-of-big-y/

Click for Larger View
Click for Larger View

[4] Rob Spencer, Case Studies in Macro Genealology, Presentation for the New York Genealogical and Biographical Society, July 2021, http://scaledinnovation.com/gg/ext/NYG&B_webinar.pdf

Rob Spencer, The Big Picture of Y STR Patterns, The 14th International Conference on Genetic Genealology, Houston, TX, March 22-24, 2019, http://scaledinnovation.com/gg/ext/RWS-Houston-2019-WideAngleView.pdf

Rob Spencer, Genetic Genealogy at the Library, Mystic and Noank Library October17, 2019, http://scaledinnovation.com/gg/mnl/mnl3.pdf ; October 10, 2019 http://scaledinnovation.com/gg/mnl/mnl2.pdf; October 7, 2019 http://scaledinnovation.com/gg/mnl/mnl1.pdf

[5] Scott Miller, Ten Facts About the American Economy in the 18th Century, George Washington”s Mount Vernon, https://www.mountvernon.org/george-washington/colonial-life-today/early-american-economics-facts/

Peter H. Lindert and Jeffrey G. Williamson, American Colonial Incomes, 1650-1774, Working Paper 19861, National Bureau of Economic Research, Cambridge, MA, January 2014, https://www.nber.org/system/files/working_papers/w19861/w19861.pdf

[6] Peter Kalm’s Travels in North America: The English Version of 1770, revised from the original Swedish and edited by Adolph B. Benson (Wilson-Erickson, 1937); reprint edition (Dover, 1966), p. 211. 

[7] Franklin, Benjamin. 1751 / 1959. “Observations Concerning the Increase of Mankind, Peopling of Countries, etc.,” in The Papers of Benjamin Franklin, Volume IV, edited by Leonard W. Larabee. New Haven, Conn.: Yale University Press. pp. 227-228

Malthus, Thomas Robert. 1798 / 1920. An Essay on the Principle of Population. London. Reprinted for the Royal Economic Society, London: 1920. pp. 105-106

[8] Rob Spencer, Case Studies in Macro Genealology, Presentation for the New York Genealogical and Biographical Society, July 2021, http://scaledinnovation.com/gg/ext/NYG&B_webinar.pdf

Rob Spencer, The Big Picture of Y STR Patterns, The 14th International Conference on Genetic Genealology, Houston, TX, March 22-24, 2019, http://scaledinnovation.com/gg/ext/RWS-Houston-2019-WideAngleView.pdf

[9] This image is the result of plugging in a GED file of my family tree into a javascript program build by B.F. Lyon, Exploring Family Trees (Beta), On-line Visualization https://learnforeverlearn.com/ancestors/?fbclid=IwAR0OJcmL83m2WRI0mnuCp26h-14btQ2MWGaTGmdpPECkP0VvkCKY4IptI9w

Features of a Web-Based Family Tree Visualization Tool, Sep 20, 2105, http://familytreeviz.blogspot.com/2015/09/features-of-family-tree-visualization.html

[10] Maciamo Hay, Haplogroup G2a, Eudepia, Last update January 2021, https://www.eupedia.com/europe/Haplogroup_G2a_Y-DNA.shtml

[11] The Y-chromosome DNA (Y-DNA) Results Colorized report headings are color-coded in two ways. First, each testing level (Y-DNA1-12, Y-DNA13-25, Y-DNA26-37, Y-DNA38-67, and Y-DNA68-111) is coded with a different shade of blue. Second, the STR (short tandem repeat) markers that have faster mutation rates and are more likely to change within the genealogical time frame are coded with a red background.

The Y-chromosome DNA (Y-DNA) results chart is color coded to show where someone in a subgroup differs from the calculated modal value for an STR (short tandem repeat) marker. For each step less than the modal value, a progressively darker shade of blue is used for the background color. For each step greater than the modal value, a progressively darker shade of pink is used for the background color.

Understanding the Y-DNA Results Colorized Report, FTDNA Help Center, https://help.familytreedna.com/hc/en-us/articles/4503464738319#accessing-the-y-dna-results-colorized-report-0-0

[12] The GD estimates and estimated number of Generations is based on FTDNATiP™ Reports, Most Recent Common Ancestor Time Predictor based on Y-STR Genetic Distance

Understanding Y-DNA Genetic Distance, FTDNA Help Center, https://help.familytreedna.com/hc/en-us/articles/6019925167631-Understanding-Y-DNA-Genetic-Distance

Concepts – Genetic Distance, DNAeXplained – Genetic Genealogy,, Blog, 29 June 2016, https://dna-explained.com/2016/06/29/concepts-genetic-distance/

[13] Time Predictor Estimates related to FTDNATiP™ Reports:

The Time Predictor (TiP), or FTDNATiP™, is a proprietary program that incorporates Y-chromosome DNA STR mutation rates to increase the power and precision of estimates of Time to Most Recent Common Ancestor (TMRCA). It is a tool provided by FTDNA  which allows for a probabilistic comparison between two Y-STR haplotypes to determine the time to the most recent common ancestor (TMRCA). The program incorporates marker-specific mutation rates to increase the power and precision of the TMRCA estimates.

[14] Rob Spencer, Case Studies in Macro Genealology, Presentation for the New York Genealogical and Biographical Society, July 2021, http://scaledinnovation.com/gg/ext/NYG&B_webinar.pdf

Rob Spencer, The Big Picture of Y STR Patterns, The 14th International Conference on Genetic Genealology, Houston, TX, March 22-24, 2019, http://scaledinnovation.com/gg/ext/RWS-Houston-2019-WideAngleView.pdf

[15] John and Sheila Rowlands, The Use of Surnames, Chapter 4, Patronymic Naming – A Survey in Transition, Llandysul, Ceredigion: Gomer Press, 2013, Figure 4-3: Decay in the use of patronymic naming to the 10% level, Page 56

[16] Shiela Rowlands, Sources of Surnames in John and Shiela Rowlands, ed, Stages in Researching Welsh Ancestry. Bury, England: The Federation of Family History Societies Publications Ltd., 1999. Pages 153 and 159

Although we are focused on individuals with the Griffith surname in the 1700’s in the American colonies, the prevalence of the Griffith surname has been documented in Wales in the 1800’s. Based on an analysis of census data in Wales in 1850, the top ten most common names represented approximately 80 percent of the Welsh population. While these names were common, it does not imply they were related. 

The result of using similar names as surnames resulted in the lack of diversity in surnames in Wales, see: John Rowlands, The Homes of Surnames in Wales in John Rowlands and Shiela Rowlands, ed, Stages in Researching Welsh Ancestry. Bury, England: The Federation of Family History Societies Publications Ltd., 1999. Page 162

Durie, Bruce, Welsh Genealogy, Stroud, United Kingdom: The History Press, 2013, Page 27

John Rowlands, The Homes of Surnames in Wales, in John and Shiela Rowlands, ed, Stages in Researching Welsh Ancestry. Bury, England: The Federation of Family History Societies Publications Ltd., 1999. Page 162-164

John and Sheila Rowlands, The Use of Surnames, Chapter 4, Patronymic Naming – A survey in Transition, Llandysul, Ceredigion: Gomer Press, 2013, Pages 50-57

[17] Rob Spencer, Y STR Clustering and Dendrogram Drawing, Tracking Back: a website for genetic genealogy tools, experimentation, and discussion, http://scaledinnovation.com/gg/clustering.html

The data was from:

Family Tree DNA L-497 Project, DNA Results, https://www.familytreedna.com/groups/g-ydna/about

[18] “All things considered, 33 years per male generation is more accurate than 30 and a reasonable choice for the eras of interest in STR genealogy. ”

Rob Spencer, tMRCA Estimation from STR Data, Revisited, Tracking Back: a website for genetic genealogy tools, experimentation, and discussion, http://scaledinnovation.com/gg/gg.html?rr=strByMu

[19] David Vance, The Life of Trees   (Or:  Still Another Phylogeny Program),SAPP Tree Generator V4.25, http://www.jdvsite.com

Dave Vance, Y-DNA Phylogeny Reconstruction using likelihood-weighted phenetic and cladistic data – the SAPP Program, 2019, academia.edu, https://www.academia.edu/38515225/Y-DNA_Phylogeny_Reconstruction_using_likelihood-weighted_phenetic_and_cladistic_data_-_the_SAPP_Program

The following provides an explanation of the structure of the phylogenetic tree;

Click for Larger view

Source: David Vance, Output, The Life of Trees   (Or:  Still Another Phylogeny Program),SAPP Tree Generator V4.25, https://www.jdvsite.com/outputs/

[20] Source: Page 13 of a readable transcript of the narration in a YouTube at https://drive.google.com/open?id=1CdU…, The video is by J. David Vance, DNA Concepts for Genealogy: Y-DNA Testing Part 1, 10 Oct 2019, https://youtu.be/RqSN1A44lYU

[21] Gruffudd Genealogies: Griffi(th(n)(s)(ng) Surname DNA Project. Website no longer updated., links are not working. http://griffdna.org/pedigrees.html#griffis

“The Griffi(th)(s)(n)(ng) surname project is intended to provide an avenue for connecting the many branches of Griffith, Griffin, Griffis, and other forms of the surname. The patronymic naming system, practiced in Wales into the latter 18th century, makes this task more difficult. Evan, Thomas, Johns, Jones, Rees, Owen, and many other common Welsh names may share common male ancestors. Surnames included in the project include: Griffen, Griffeth, Griffeths, Griffets, Griffett, Griffin, Griffing, Griffis, Griffit, Griffith, Griffiths, Griffitth, etc.”

“For the results to be meaningful, participants will need to share their direct male line ancestry back to the earliest known GRIFFITH/GRIFFIN/GRIFFIS/etc., either in the form of a pedigree chart, family group sheets, or electronic GEDCOM files.  Living persons should be excluded from the documentation.”

[22] References to Abia’s marriage to Simon half indicate her name was Abiah Griffis. Baldwin, Evelyn Briggs contributed by, Marriages and Baptisms Performed by Rev. Joshua Hartt of Smithtown , Long Island, with a Sketch of his Life, New York Genealogical and Biographical Record, Vol 42, April 1911, July 1911 . Page 278.

References to Abiah burial, indicate her name as “Abiah Griffiths Haff”, Find A Grave Website, memorial no. 206641461, Hauppauge Rural Cemetery Hauppauge, Suffolk County, New York, USA

[23] Baldwin, Evelyn Briggs contributed by, Marriages and Baptisms Performed by Rev. Joshua Hartt of Smithtown , Long Island, with a Sketch of his Life, New York Genealogical and Biographical Record, Vol 42, April 1911, July 1911 .

[24] Arvilla Rogers Griffith, Obituary, Valley morning Star, 18 Sep 2014, Page 8, Harlingen, TX. PDF available.

Henry V. Griffith, Find My Grave, Memorial ID: 180803329, Plot section 47A site 49 https://www.findagrave.com/memorial/180803329/henry-v.-griffith

Arvilla Rogers Griffith, Find My Grave, Memorial ID: 136333620, Plot Section 47A Site 48 https://www.findagrave.com/memorial/136333620/arvilla-rogers-griffith

Y-DNA and the Griffis Paternal Line Part Four: Teasing Out Genetic Distance & Possible Genetic Matches from STR Tests

This is part four of a story on utilizing Y-DNA tests to gain knowledge or leads on the patrilineal line of the Griff(is)(es)(ith) family. This part of the story focuses on the analysis of Y-STR test results to possibly locate genetic ancestors.

Working with Y-STRs (and Y-SNPs) and the various types of tests and Y-DNA tools requires covering the topics of genetic distance,  modal haplotypes, ancestral haplotypes and the Most Recent Common Ancestor.

Most Common Ancestor: A Peculiar Concept

A number of genetic studies argue that all humans are related genealogically to each other over what can be considered as surprisingly short time scales. [1] Few of us have knowledge of family histories more than a few generations back. Moreover, these ancestors often do not contribute any genetic material to us [2]

In 2004 mathematical modeling and computer simulations by a group of statisticians indicated that our most recent common ancestor probably lived no earlier than 1400 B.C. and possibly as recently as A.D. 55. Additional simulations, taking into account the geographical separation of continents and islands and less random patterns of mating in real life suggest that some populations are separated by up to a few thousand years, with a most recent common ancestor perhaps 76 generations back (about 336 BCE), though some highly remote populations may have been isolated for somewhat longer [3]

The most recent common ancestor of a group of men and the most common ancestor of man are concepts used in genetic genealogy. Their definition and explanation are not entirely intuitive. They can be difficult to comprehend and what do they actually mean. For most of us it is a bit difficult to accept or even comprehend concepts that rest on mathematics or statistics and not hard data. Archaeologists, genealogists, or historians will never uncover ancient artifacts or documentation that identify your most recent common ancestor

The idea of a genealogical common ancestor resists attempts to demonstrate its existence with a genetic, DNA equivalent. As special as either of ‘these recent individuals’ are within our genealogy, it is very likely that most living people have inherited no DNA from these individuals at all.  

This may seem like a paradox: a genealogical ancestor of everybody, from whom most of us have inherited no DNA. It reminds us that genetic and genealogical relationships are different from each other. Many close genealogical relatives are nonetheless genetically and culturally very different from each other. Fifth cousins are not far apart genealogically, but they sometimes share no DNA from their common genealogical ancestors at all. [4]

The following video provides an excellent overview of the interplay between different concepts of genealogy and their implications. The video also touches on the concept of common ancestor, identical ancestors point (IAP), or all common ancestors (ACA) point, or genetic isopoint, and the most recent ancestor. [5]

Genetic Distance

While I brought up the concept of most common ancestor for discussion, our main concern is really with something that is more manageable to comprehend in terms of genetic distance: genetic distance based on the most recent common ancestor. It still might be confusing but not mind blowing.

Genetic distance, is a concept used more as an operational concept by FamilyTree DNA (FTDNA). It is a concept that ranks individual test kits according to how close they appear to be to each other based on the number of allele differences on designated short tandem repeats (STRs). 

Genetic distance can also be calculated using Single-nucleotide polymorphisms (SNPs) by comparing the time distance between different haplogroup branches. For the most part the concept is used in the context of comparing genetic test results between two or more Y-STR test kits to determine if they are genetically ‘closely related’. [6]

Genetic distance is based on the analysis of STR data, is the result of calculating the number of mutation events which have occurred between two or more individuals in their respective haplotypes. The more STR’s sampled and compared, the more reliable is the estimate of genetic distance.  

Most Common Recent Ancestor

In genetic genealogy, the most recent common ancestor (tMRCA) of any set of individuals is the most recent individual from which all the people in the group are directly descended. [7] Estimating TMRCAs is not an exact science.  Because it is not an exact science, questions and answers regarding TMRCA should be phased in general terms. For example, is the MRCA likely to be within the time of surnames or is the MRCA more likely to be in the 1`700’s or the 1600’s. Generally, TMRCA concept can be used to give a working theory or hypothesis about which general time frame the common ancestor may have lived. 

The results of various type of analyses that calculate genetic distance will point to the most recent common ancestor of a group of men.

The information in Table One was introduced in Part Three of this story and will be used as a basis for discussing my path of discovery for genetic ancestors using the concept of genetic distance and tMRCA.  The table displays Y-Chromosome DNA (Y-DNA) STR results for testers in the L-497 Haplogroup project. As reflected in Illustration One, twelve test kits were grouped together based on how they tested for specific SNPs associated with branches in the haplotree.

Illustration One: The One Two Punch of SNP then STR Analysis

Specifically, Table One provides STR data on my haplotype (STR signature), which is highlighted in the table, for 111 sampled STR values. My results are grouped with eleven other men based on our similarity in our respective STR haplotype signatures. We also share similarities in SNP tests and have been grouped in the G-BY211678 haplogroup. 

Table One: 111 STR Results for G-L497 Working Group Members within the G-BY211678 Haplotree Branch 

Source: FTDNA DNA Results for Y-DNA Group Members of Haplogroup L-497 within the FY211678 haplotree branch | Click for Larger View

The table provides the modal haplotype for the twelve individuals (re: third row) and the minimum and maximum values for each of the STRs listed in the table. FTDNA uses the concept of genetic distance (GD) to compare and evaluate genetic resemblance of two or more STR haplotypes. It is at this point we start to compare STRs among potential test kits.

Genetic Distance: What Does It Mean, How is it Used & How to Portray It

haplotype (haploid genotype) is a group of alleles in an organism that are inherited together from a single parent. [8] 

Unlike other chromosomes, Y chromosomes generally do not come in pairs. Every human male (excepting those with XYY syndrome) has only one copy of that chromosome. This means that there is not any chance variation of which copy is inherited, and also (for most of the chromosome) not any shuffling between copies by recombination. Unlike autosomal haplotypes, there is effectively not any randomization of the Y-chromosome haplotype between generations. A human male should largely share the same Y chromosome as his father, give or take a few mutations; thus Y chromosomes tend to pass largely intact from father to son, with a small but accumulating number of mutations that can serve to differentiate male lineages.

Haplotypes in Y-DNA testing typically compare the results of Y-25, Y37, Y-67, or Y-111 STR tests. Table Two is an example of my haplotype for the Y-111 test. The haplotype basically represents the unique string of values for each of the STRs that compose the test. They number essentially do not mean much by themselves. They take on meaning when you compare them with other testers or pool my results with others to concoct dendrograms and higher level statistical analyses. 

Table Two: Example of the Y-111 Haplotype for James Griffis

Y-111 Haplotype of James Griffis | Click for Larger View.

modal haplotype is an ancestral haplotype derived from the DNA test results of a specific group of people, using genetic genealogy. Within each FTDNA work group that is based on haplogroups, surnames, geographical area, or other categories, typically test results are grouped on the basis of the most recent common ancestor that is based on a modal haplogroup.  [9]

The modal haplotype is found on the third row of the table One. My results are found on the fourth row of the table for Kit number 851614. Click on the image for a viewable version. The table also provides the minimal allele values for each STR marker and the maximum allele values for each marker for comparison. 

The ancestral haplotype is the haplotype of a most recent common ancestor (tMRCA) deduced by comparing descendants’ haplotypes and eliminating mutations. A minimum of three lines, as distantly related as possible, is recommended for deducing the ancestral haplotype. This process is known as triangulation.  For FTDNA testing, ancestral haplotype basically refers to the haplotype of the tMost Recent Common Ancestor (tMRCA). In genetic genealogy, the Most Recent Common Ancestor (tMRCA) is the ancestor shared most recently between two individuals. [10]

For Y-DNA, the Most Recent Common Ancestor (tMRCA) is defined as the closest direct paternal ancestor that two males have in common . One of the questions all genealogists seek to answer is when a mutation occurs. We want to know when a mutation occurs and how closely we are related to others that have similar SNP or STR mutations. Unfortunately, that question, without traditional genealogical ancestral information, is very difficult to answer. 

For the past two decades, many researchers have attempted to reliably answer that question. The key word here is ‘reliably’. The general consensus is that the occurrence of a SNP is someplace, on average, between 80 and roughly 140 years. The topic is hotly debated, and many factors can play into SNP age calculations. [11]

Since STRs mutate faster than SNPs and can also have a likelihood of mutating back to an original configuration, the estimate of the age of a STR mutation is challenging and depends on the specific STR since they each mutate at different rates. Given the nature STRs, the strategy for locating tMCRA with STRs relies on the concept of genetic generations (e.g. genetic distance). Translating genetic distance to years relies on statistical probabilities based on (a) the specific STR markers tested and (2) the number of STR markers used in calculations.

FTDNA Genetic Distance and Y-DNA STRs: Individual Matches

The main feature of FamilyTreeDNA’s Y-STR tests (Y-37 through Y-111) are finding Y-DNA matches. Like most DNA tests for genealogy, the test is most useful when compared to other people. The key question is, “When was the last common ancestor with this match?” When that is not obvious from comparing known genealogies, the genetic distance is the metric used to compare and estimate how far back in time the connection goes to identity the Most Recent Common Ancestor (tMRCA). Is the connection in recent times, just behind that genealogical brick wall, or in ancient, prehistoric times?

The FTDNATiP™ Report (TiP for Time Predictor) translates the Genetic Distance (GD) statistic into a time unit in predicted ‘years ago’. Depending on the average rate of mutation for sampled marker STRs, the number of differences between two samples (individuals) grows larger as the number of generations back to a common ancestor increases. FTDNA uses this idea to limit the number of matches shown in their match reports. As reflected in Table Three, if you have a 12 marker test (Y-12 STR test), their cut off is a genetic distance of one (one mutation difference), for their Y-37 marker tests the report cut off is at a genetical distance of 4, at 67 markers it is 7, and at 111 markers the report cut off is 10. [12]

Table Three: FTDNA Limits on Genetic Distance Based on Level of STR Test

Test LevelGD Limit for Matches
Y-120 or 1 if they are in the
same working
group project
Y-252
Y-374
Y-677
Y-11110

In general, the closer the match in haplotypes between two individuals, the shorter the time back to a most recent common ancestor. For instance, if two individuals share the allele values for 35 out of 37 STR markers, they almost certainly share a more recent common ancestor than two individuals who share 25 out of 37 markers.

When it comes to calculating the genetic distance of a common ancestor, which STRs are different between the two individuals is more important that how many differences there are.  This is due to the fact that STRs can behave differently from their expected mutation rates and because some STRs mutate faster than others. Regardless of whether one takes a 12 37, or 111 STR marker test, a distance of four matters more based on the mutation rates for each of the four markers that are different. 

The following tables indicate the mutation rates for each of the STRs that are used for the various STR tests. [13]

Table Four: Mutation Rates for STRs 1 Through 37

STRs 1 through 37 | Click for Larger View

Table Five: Mutation Rates for STRs 38 – 67

Table Six: Mutation Rates for STRs 68 – 111

As mentioned earlier, calculating the Time to Most Recent Common Ancestor is based on probability and is not an exact science. We can identify the most likely time that a common ancestor might have lived, but there will always be a degree of uncertainly. It is better to think of “the Most Recent Common Ancestor” (tMRCA) as a range of time rather than a point in time. [14]

The following four charts show (noted by the dark line) the average number of generations that Y-DNA matches will share a common ancestor based on genetic distance. The statistical confidence levels are based large population samples and the two lighter lines show a band or range in which 95 percent of the matches will fall. The charts indicate where the FTDNA ‘cut off’ occurs. Notice that as you test more STR markers, the genetic distances also go up for the same number generations. For the Y chromosome these rates assume a 31 year generation and basing years ago from a 1955 “present date”. [15]

As illustrated in the following four illustrations, the statistical variabiability in determining the range of generations based on the concept of genetic distance can vary widely. Even comparing genetic distance with 111 STR test results, one will have a wide statistical variance. A genetic distance of 2 for a Y-111 comparison will mean that the match is within a 95 percent confidence interval of 2-10 generations. If a generation is around 31 years, then the match is equivalent to 62 – 320 years. Translating this range to ‘years before present would be 1955-62= 1893 CE and 1955-320= 1635 CE. That can be a wide range if you are looking for genetical matches.  [16]

Illustration Two: Relationship of Genetic Distance to Generations at Y 12

Illustration Three: Relationship of Genetic Distance to Generations at Y37

Illustration Four: Relationship of Genetic Distance to Generations at Y67

Illustration Five: Relationship of Genetic Distance to Generations at Y111

Up until very recently, there were two methods to determine the GD.: the Step-Wise Mutation Model and the Infinite Allele Model.  [17] In 2022, FTDNA released Age Estimates based on the Big Y-700 test. test results The millions of slow-mutating Y-SNP markers tested by Big Y together with the faster-mutating but fewer Y-STR markers derived revised the Time to Most Recent Common Ancestor (TMRCA) estimates of each branch on the Y-DNA haplotree. [18]  Also in 2022, FTDNA updated FTDNATiP™ Report using Big Y haplotree TMRCA estimates from hundreds of thousands of pairs of Y-STR results from Big Y testers and built models to predict the most likely TMRCA ranges for each Y-STR marker level and genetic distance. [19]

Most mutations only cause a single repeat within a STR marker to be added or lost. For these markers, the Step-Wise Mutation Model is used. For example in Table Seven, comparing my results (Kit Number 851614) with Kit number 125476, who also lists a William Griffis as a Paternal Ancestor, the values of two STR markers differed by one value (see below), which means our GD is 2. 

Table Seven: Comparison of Two STR Markers

Kit NumberDYS389ii
Allele Value
DYS576
Allele Value
8516142818
1254762917

In some cases, an entire marker is added or deleted instead of a single repeat within a marker. This is believed to represent a single mutation in the same way that the addition or subtraction of a repeat is a single mutation event. For this reason, FTDNA uses the Infinite Allele Model in these cases. When an STR simply does not exist in an individual, this is called a null value. When a marker is missing, the value is listed as 0. 

Multi-copy STR markers appear in more than one place on the Y chromosome. These are reported as the value found at each location, separated by hyphens. For example, in table one you may see DYS464= 12-13-13-13 or 12-12-13-13-13 or 12-13-13-13-13-13 . This means that the STR marker DYS464 has a unique number of repeats in each location. These locations are usually referred to as DYS464a, DYS464b, DYS464c, etc.

An example of this situation is illustrated in Table Eight by comparing my STR results in Table One (Kit Number 851614) with Kit Number 31454 (whose Paternal Ancestor is William Wamsley) and 285488 (whose self reported paternal ancestor was George Williams).:

Table Eight: Comparison of Multi-Copy STR Markers

Kit NumberDYS
464a
DYS
464b
DYS
464c
DYS
464d
DYS
464e
DYS
464f
Total
GD
85161412131313
3145412121313132
2854881213131313132

Within multi-copy markers, there are two types of mutations, or changes, that can occur: marker changes and copy changes. Marker changes (changes in how many repeats are within a marker) are counted with the Step-Wise Mutation Model. Copy changes (changes in the number of markers, regardless of how many repeats are in each) are counted with the Infinite Allele Model. 

In the example illustrated in Table Eight, if we compare Kit 31454 to my kit 851614, the allele value for DYS464b is different by one (marker change) and also 31454 has an additional copy (DYS464e), which totals to a genetic distance of 2. Comparing kit 285488 with my kit reveals no marker changes in DYS464a-d but two additional copy changes (DYS464e-f), which totals to a GD of two.

Adding together the GD for each marker in two people provides the overall GD for those two people. When a GD becomes ‘too great’, it is unlikely that the two people share a common ancestor within a ‘genealogical timeframe’, so FTDNA establishes a upper level limit for reporting matched based on GD.

Table Nine provides a practical example of FTDNA’s strategy of comparing the differences between haplotypes of individual test results based on similar haplogroups. I have listed the surname of each of the testers and the STR test they completed (re: Y-37, Y-67, Y-111, or Big Y 700 test. The table also provides information on the most recent haplogroup branch their respective tests were able to document. A Big Y 700 test provides results for 700 STR and therefore can provide the most granular test results for haplogroup designation. The table also indicates the self reported earliest known paternal ancestor for the tester. 

Table Nine: STR Haplotype Matches with James Griffis Based on Y-37 Test

Kit
No.
SurnameSTR 
Markers 
Tested
Genetic
Distance
(GD)
Likely
Common
Ancestor
(Genera-
tons) [12]
MRCA
Based 
on GD
[12]
Earlest
Known 
Ancester
125476Griffith372 Steps8 (2-20)1650 CEWilliam
Griffis
39633Compton372 Steps8 (2-20)1650 CEUnknown
154471Williams1114 Steps3(7-15)1700 CEWilliam
Williams
285488Williams7004 Steps3(7-15)1700 CEGeorge
Williams
294448Williams1114 Steps3(7-15)1700 CEGeorge
Williams
285458Williams1114 Steps3(7-15)1700 CEGeorge
Williams
36706Williams674 Steps11(4-22)1500 CEWilliam
Williams
149885Gough374 Steps14(6-28)1300 CEGough
Source: FTDNA myFTDNA Y-DNA Match Results for James Griffis

As illustrated in Table Nine, although the tester whose last name is Griffith (first. row of the table) only tested for the Y-37 test, his test results are 2 steps different from my test results. If we look at Illustration Three above, this means I and Mr. Griffith share a common ancestor around 8 generations ago or between 2 to 20 generations.. Eight generations would be around the revolutionary war period. 

There is another test kit that is 2 steps different from my test kit results. The test kit 39633, who has a surname of Compton appears to be as close as Mr. Griffith. I do not have any traditional genealogical documentation that references an individual with the last name of Compton. Rather than dismiss the results, one needs to look ‘outside the box’ in terms of critically analyzing the results. I may need to reach out to this gentleman to see what potential connections we might have. Also, based on the statistical confidence levels associated with the Y-32 STR tests, the MRCA may be as far back as 20 generations or 620 years ago which is around 1400 CE.

The remaining six testers are four steps different from my test results. While I know there are no individuals who are related in the past three generations, perhaps 15 to 22 generations back there might be a common ancestor. The outer range would be around 682 years ago or around 1340 CE. which would be before the use of surnames.

Based on the results, further research into the background of Mr. Griffith, whose earliest known ancestor was a ‘William Griffis from Hungton, NY” may lead to promising results! 12 generations would be around the early colonial era (1650). It may also be worthwhile to look into the Williams’ connections!

Phylogenetic Trees: Graphic View of Genetic Distance at the Lineage Level

In addition to analyzing and providing Y-DNA test results, FTDNA provides a wide platform of ways in which DNA results are analyzed and the results are packaged for consumers to identify possible genetic matches. There are also a number of analytical tools that have been developed by individuals that compliment or enhance the ability to assess genetic distance. 

I can complement the second stage of an analysis by reviewing the results of genetic distance that we just discussed in a number of program generated mutation history trees. These types of programs give a pictorial representation of how the different members of a lineage may be related. 

The branching pattern derived from the DNA mutations may very well correspond to the branching pattern that one might see in a traditional family history tree if we were able to trace it all the way back with documentary evidence to the MRCA (Most Recent Common Ancestor). The Mutation History Tree can give us important clues regarding which individuals are likely to be on the same branch of the overall tree, and who is more closely related to whom. This in turn can help focus further documentary research.

One type of mutation history tree has been developed by David Vance that uses FTDNA data that creates a Y-DNA phylogenetic tree. The program is relatively easy to use and graphically provides an intuitive approach to visualize the possible genetic relationships between various DNA test results. The program is referred to as the SAPP analysis (Still Another Phylogeny Program). The current version that was used in my analysis was SAPP Tree Generator V4.25. [20]

The program uses STRs from any of the STR tests (e.g., Y25, Y37, Y67, Y111), to construct a Y-DNA phylogenetic tree.  It also has the ability to incorporate the SNPs found in BigY tests to fine-tune the genetic links and estimated times to the most common recent ancestor.  The program can also incorporate known names and birth dates of ancestors to further fine-tune the analysis.

The program provides:

  • STR Table. This table is included to verify the STR input. It starts with the calculated Group Modal Haplotype for your input set followed by all the input kits with the off-modals colored.
  • Original Genetic Distance Table. This table calculates genetic distances (GDs) from the input STR results. It should match closely with GD calculations from other tools and commercial companies.
  • Adjusted Genetic Distance Table. This table re-calculates the GDs based on the tree that SAPP has just calculated. It will correct for any convergence that may have occurred in the calculated tree. 
  • Kit to SNP/Genealogy Cross-Reference. This table summarizes the input SNP and Genealogy data showing the +. -. or ? status against the various kits. 
  • The Image or Web version of the Tree File. The program creates a downloadable file containing the phylogenetic tree. Normally the tree is drawn as a graphic, as indicated in Illustration Six.

Illustration Six: Explanation of the SAPP Phylogenetic Tree

Utilizing the STR results, SNP data, and self reported paternal ancestor information for the 12 tests kits found in Table One, the following phylogenetic tree was created (click on the image of the thumbnail of the tree to be able to actually see the table). I have provided a PDF version of the Phylogenetic Chart which allows you to enlarge the image to get a better view.

Illustration Seven: Phylogenetic Tree Results for FTDNA STR Test Results for Individuals within the G-BY211678 Haplogroup (Click for Larger View)

Click for Larger View

The phylogenetic tree reveals three major genetic groupings of the 12 test kit results. One of those groupings tie my results (FTDNA Kit Number 851614) with an individual whose surname is Griffith (FTDNA Kit Number 285458) and claims the same paternal ancestor, William Griffis see Illustration Eight.

Illustration Eight: Close Up of Phylogenetic Tree

The following are the original and adjusted genetic distance tables generated by the SAPP program. The number of STRs tested are listed on the diagonal in blue. Cell colors refer to the number of STRs tested – cells of different colors are not directly comparable.
Red numbers indicate where adjusted genetic distances are different from original calculation.

Table Ten: SAPP Generated Original Genetic Distance between the 12 Test Kits.

Table Eleven : SAPP Generated Original Genetic Distance between the 12 Test Kits.

Based on the SAPP results, consistent with the FTDNA analysis, it is estimated that the most recent common ancestor between me and Mr. Griffith is approximately 8 generations or 248 years ago (estimating a generation to be 31 years) which would mean the MRCA was born around 1772. The birth date of William Griffis was 1736.

The results of the SAPP analysis suggests that there possibly may be an additional three haplotree branches, based on differences between STR haplotypes among the twelve test kits.

The phylogenetic chart indicates that the MRCA for all of the twelve test kits is estimated at 23 generations.  The MRCA was born around 1500 CE for the G-BY211678 haplogroup. The Node #13 of which I and Mr. Griffith are representatives has the strongest connection in the tree. M=Test kits that indicates the ancestral person as William Williams or William Walmsley appear to have a MRCA 3 generations ago (born around 1850).

Genetic Distance at the Macro Level: Distance Dendrograms

The creation of dendrogram is another tool to use when analyzing STR data. Dendrograms can provide insights into macroscopic patterns in Y-DNA genetics and possible genetic matches of present day Y-DNA testers. The diagram based approach of a dendrogram is visually intriguing. Distance dendrograms are software-generated diagrams that convey relationships based on distance measured either in years or generations. Statistically, the dendrograpms used in the present context for genealogy are constructed by hierarchic clustering and the UPGMA method and are more focused on macroscopic genetic patterns. They complement other tools that focus on family level matches. [21]

Up until this point in the story we have discussed computing tMRCA based on the concept of genetic distance (GD). This sort of pairwise tMRCA analysis is subject to a signfiicant range of statistical uncertainty (as reflected in the above tables for generational distance). 

A tMRCA can also be calculated between a single DNA tester and the estimate pattern of a chosen ancestor using a modal haplotype. If you have a large enough set of DNA test kits to sample, the ancestral haplotype will be close to that unknowable MRCA. However, this type of averaging still creates a wide level of variance for individual contemporary testers to compare their results with this ‘statistical archetype’. 

The dendrograms generated in Rob Spencer’s model is based on a ‘whole-clade’ estimation of the MRCA. The MRCA for an entire clade (haplogroup branch) can be determined based on a common ancestor or a target SNP. The distribution of pairwise MRCA’s for a number of selected DNA kits in a given clade can be fit into a statistical curve fitting process (e.g. lognormal distribution). This curve fitting process is done on a specific group of DNA kits using statistical methods that are way above my pay grade. [22]   

The scale of the data and graphics can reveal large scale, high-level patterns of when one person became the descendant of all others (single founder clades), patterns of descent from a single colonial founder in the America (typically one person is the descendant of all in America), and other demographic patterns that are not apparent using other methods of presenting DNA test results.  

Dendrograms are ‘close cousins’ to family trees. The Y-STR Dendrogram is a diagram similar to a family tree. Individual DNA testers are the dots at the right (if the dendrogram is horizontal) or at the bottom (if the Dendrogram is vertical). Time moves backward to the left (if horizontally depicted) or down and up( vertically presented). On a traditional family tree, branch points are actual ancestors. In the dendrogram the branch points are generally not specific people but points in time when genetic mutations or changes occurred. In some cases, with good paper genealogy, branch points can be matched to specific ancestors. [23]

Looking at dendrograpm from another angle, they are graphic renderings of a statistical analysis which compares the differences of STR allele values between a group of DNA testers to determine the most recent common ancestors (tMRCA) between a group of testers. One of the key properties of a distance dendrogram is that if the input distances are accurate and consistent, then the graphic will completely and correctly represent a family tree. If we had a sufficient set of testers who had done DNA tests and tMRCAs could be calculated for all pairs with complete accuracy, then the dendrogram would be an accurate family tree. 

You can demonstrate the relatiohsip between dendrograms and family trees for yourself with the Distance Tree Introduction interactive tool, and also for larger and more realistic family trees with the Family Simulator, both created by Rob Spencer. 

The major limitation to the accuracy of the dendrogram trees is the statistical and random nature of STR mutations. In general, dendrograms constructed from Y12 or Y37 data will be reliable, while those built with Y111 or Big Y700 data data will be sufficient to see large-scale patterns (“macro genetics”) and in many cases can be close approximations to the true family tree. [24]

One important difference between a dendrogram and a family tree is that a dendrogram defines only the “leaf nodes”. A dendrogram does not “know” that there are other nodes that represent people on the diagram. The joining nodes or points are mathematical constructs. Every joining-point or “T” junction in the diagram corresponds to a specific genetic ancestor. 

“(Dendograms) are very reliable for exclusion: you can say with very high confidence that two people are not related if there is a strong mismatch of their STR patterns. This is the forensic use of DNA: it’s very powerful in proving innocence while less decisive about proving guilt.” [25]

“Most of us use Y STR data locally to explore personal matches and to help in building family trees. But STRs can tell us much more when we sit back and take a long look. In this talk we use an efficient way to visualize thousands of kits at once. The large-scale patterns explain “convergence”, illuminate ancient, feudal, and colonial expansions, pick apart Scottish clans, identify American immigrant families, allow accurate relative clade dating, let us see the onset of surnames, and reveal the power law distribution of lineages.” [26]

Utilizing STR and SNP data, dendrograms can spot American Immigrant families based on the shape of the dendrogram. Typically there is a gap of 10 plus generations to the next ancestor and an expansion around 5-15 generations ago. [27] Similarly, the advent of surname usage can appear in dendrogram renditions of Y-DNA data. You should expect a common surname only for branches with a tMRCA 25-30 generations ago.  Otherwise connections between branches with surnames are essentially random.  [28]

Illustration Nine provides a dendrogram of the entire group of FTDNA test kits for the L-497 Haplogroup work group. It includes testers who have minimally completed a Y37 STR test. The L-497 subclade, of which the Griff(is)(es)(ith) paternal line is a part, genetically branched off around 8900 BCE, the man who is the most recent common ancestor of this line is estimated to have been born around 5300 BCE. There are about 1,760 FTDNA based DNA tested descendants, and they specified that their earliest known origins are from Germany, England, United States, and 53 other countries.  I included the entire group of test results to show the general shape and patterns revealed in the dendrogram.

STR distance dendrograpms usually contain clear and distinct clades, which are sets of men with a common ancestor. Such clades are characterized by a curved top boundary. in the dendrogram. This is what gives the dendrogram its characteristic ‘slope shape’. If we had test results of all family members the dendrogram would be more square shaped and resemble a family tree. Since that is impossible, there are obviously gaps and the sloping tops for respective clades of the dendrogram is due to the statistical range of the STR mutations and the history of a given haplogroup. . 

While the G haplogroup was one of the dominant lineages of Neolithic farmers and herders who as a second wave into Europe, migrated from Anatolia to Europe between 9,000 and 6,000 years ago, they were overtaken by the R Haplogroup as part of a third wave of human migration into Europe and are consequently are presently a minority genetic group in Europe. The male lineages represented by the G haplogroup line are diminished and this is represented in dendrograms with long thin lines through time representing fewer male descendants.

I have highlighted distinctive clades in Illustration Nine as well as indicating the relative position of two possible descendants of William Griffis. To get a better view of this long Dendrogram, I have included a PDF version which allows one to increase the magnification of the image.

Illustration Nine: Dendrogram of FTDNA Y37 to Big Y Test Results for Members of the L-497 D-DNA Group 

Y-DNA Dendrogram: L-497 Work Group Y37 and up 
Click for larger View

If we look a bit closer at the results that are roughly highlighted in Illustration Nine, we can still see the “slope of an approximately family genetic clade structure” for individuals that have a Williams surname. This is reflected in illustration 10. My line of patrilineal descendants have a MRCA with this Williams clade around 14 generations ago. This MRCA was born would be about 434 years before present or about 1488 CE.

Illustration Ten: Dendrogram of FTDNA Y37 – Big Y Test Results for Members of the L-497 D-DNA Group – Blow-Up Portion Where My Test Kit is Located

Click for Larger View

The dendrogram reinforced the connection with Mr. Griffith’s test kit. The dendrogram shows that we have a common ancestor about 8 generations ago. I highlighted our two kits in the dendrogram.

An alternative view of the dendrogram in Illustration Ten is provided by tightening the generational time scale, is provided in Illustration Eleven. It is the same data but the horizontal scale of the dendrogram has been shortened.

Illustration Eleven: Dendrogram of FTDNA Y37 – Big Y Test Results for Members of the L-497 D-DNA Group – Blow-Up Portion Where My Test Kit is Located, Shortened Time Horizontal the scale

Y-DNA Dendrogram: L-497 Work Group Y37 and up 
Click for larger View

Comparing the SAPP and dendrogram results with the Genetic Distance results reveal similarities. They both point to a genetic relationship with Kit 285458 (Griffith) with my Kit (285614). Both analyses point to a MRCA between our kits at 8 generations.

What’s Next

The next part of the story provides the results of corroborating a Griff(is)(es)(ith) relative, Henry Vieth Griffith, through the analysis of Y-DNA STRs!

Sources

Feature Image of the story is a dendrogram of comparing test kits results of Y-STR tests. Dendrograms are software-generated diagrams that convey relationships based on distance measured in generations.  The dendrogram graphically portrays th genetic distance between individuals who are genetically related to me in the past 20 gnerations (e.g. the past 660 years). It is a graphic and mathematical confrmation of my conneection with Henry Vieth Griffith.

[1] Chang J (1999) Recent common ancestors of all present-day individuals. Advances in Applied Probability 31: 1002–1026.

Rohde DLT, Olson S, Chang JT (2004) Modelling the recent common ancestry of all living humans. Nature 431: 562–566.

Rohde DL, Olson S, Chang JT; Olson; Chang (September 2004). “Modelling the recent common ancestry of all living humans” (PDF). Nature431 (7008): 562–66. Bibcode:2004Natur.431..562RCiteSeerX 10.1.1.78.8467doi:10.1038/nature02842PMID 15457259S2CID 3563900

[2] Kevin P Donnelly, The probability that related individuals share some section of genome identical by descent. Theoretical Population Biology Vol 23: Issue 1, 1983, Pages 34–63. https://www.sciencedirect.com/science/article/pii/0040580983900047

[3] Rohde DLT, Olson S, Chang JT (2004) Modelling the recent common ancestry of all living humans. Nature 431: 562–566.

[4] John Hawks, When did humankind’s last common ancestor live? A surprisingly short time ago, 10 Jul 2022, John Hawks Weblog, https://johnhawks.net/weblog/when-did-humankinds-last-common-ancestor-live/

[5] Identical ancestors point , Wikipedia, This page was last edited on 17 December 2022, https://en.wikipedia.org/wiki/Identical_ancestors_point

[6] Genetic Distance, Wikipedia, This page was last updated 7 Dec 2022, https://en.wikipedia.org/wiki/Genetic_distance

Genetic distance, International Society of Genetic Genealology, Page was last updated 31 Jan 2017,  https://isogg.org/wiki/Genetic_distance

Understanding Y-DNA Genetic Distance, FTDNA Help Center, https://help.familytreedna.com/hc/en-us/articles/6019925167631-Understanding-Y-DNA-Genetic-Distance

[7] The Most Recent Common Ancestor, International Society of Genetic Genealology Wiki, This page was last editd on 31 Jan 2017, https://isogg.org/wiki/Most_recent_common_ancestor

David Vance, Chapter 16, Estimating Ages to Common Ancestors, David Vance, The Genealogist Guide to Genetic Testing, 2020

[8] Haplotype, Wikipedia, This page was last edited on 11 February 2023, https://en.wikipedia.org/wiki/Haplotype

[9] Modal Haplotype, Wikipedia, This page was last edited on 6 April 2020, https://en.wikipedia.org/wiki/Modal_haplotype

[10] Ancestral Haplotype, International Society of Genetic Genealology Wiki, This page was last edited on 31 January 2017, https://isogg.org/wiki/Ancestral_haplotype

[11] Most Recent Common Ancestor, Glossary of Terms, FTDNA Help Center , https://help.familytreedna.com/hc/en-us/articles/4418230173967-Glossary-Terms-#m-0-12

Most recent common ancestor, International Society of Genetic Genealogy Wiki, page was last edited on 31 January 2017, https://isogg.org/wiki/Most_recent_common_ancestor

Most recent common ancestor, Wikipedia, page was last edited on 20 October 2022, https://en.wikipedia.org/wiki/Most_recent_common_ancestor

What is YFull’s subclade age methodology, page accessed 9 Aug 2022, https://www.yfull.com/faq/how-does-yfull-determine-formed-age-tmrca-and-ci/

The results and methodology used for determining ages from Big-Y SNPs can also be found in Iain McDonald’s U106 analysis. Read the PDF version at http://www.jb.man.ac.uk/~mcdonald/genetics.html which are updated several times a year.   

Iain McDonald, Improved Models of Coalescence Ages of Y-DNA Haplogroups. Genes. 2021; 12(6):862. https://doi.org/10.3390/genes12060862

Poznik, G., Xue, Y., Mendez, F. et al. Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences. Nat Genet 48, 593–599 (2016). https://doi.org/10.1038/ng.3559 for PDF version: https://pure.mpg.de/rest/items/item_2307728/component/file_2307727/content

Shigeki Nakagome, Gorka Alkorta-Aranburu, Roberto Amato, Bryan Howie, Benjamin M. Peter, Richard R. Hudson, Anna Di Rienzo, Estimating the Ages of Selection Signals from Different Epochs in Human History, Molecular Biology and Evolution, Volume 33, Issue 3, March 2016, Pages 657–669, https://doi.org/10.1093/molbev/msv256

Kun Wang, Mahashweta Basu, Justin Malin, Sridhar Hannenhalli, A transcription-centric model of SNP-Age interaction, PLOS Genetics doi: 10.1371/journal.pgen.1009427 , bioRxiv 2020.03.02.973388; doi: https://doi.org/10.1101/2020.03.02.973388

Zhou, J., Teo, YY. Estimating time to the most recent common ancestor (TMRCA): comparison and application of eight methods. Eur J Hum Genet 24, 1195–1201 (2016). https://doi.org/10.1038/ejhg.2015.258

Most recent common ancestor, International Society of Genetic Genealogy Wiki, page was last edited on 31 January 2017, https://isogg.org/wiki/Most_recent_common_ancestor

Most recent common ancestor, Wikipedia, page was last edited on 20 October 2022, https://en.wikipedia.org/wiki/Most_recent_common_ancestor

For specific information on history of the haplotree and related nomenclature, see also: International Society of Genetic Genealogy, Y-DNA Haplogrouptree 2019 – 2020, Version: 15.73   Date: 11 July 2020, https://isogg.org/tree/

YFull has a documented system to estimate SNP ages. This is how to get their estimate:

Go to YFull’s SNP search page; 2) Enter a SNP name and click the Search button; 3) A green hyperlink, labeled with a haplotree branch name (e.g., “R-L47”), should be displayed. Click on it; 4) You should now see a branch of the haplotree. Typically, this branch will have two dates: (a) The “formed” date is an estimate of when this branch began to diverge from its surviving siblings. (Extinct siblings are unknowable and therefore ignored.) (b) The “TMRCA” date is an estimate of when this branch’s surviving children began to diverge from each other. (Again, extinct lineages are ignored.)

[12] The GD estimates and estimated number of Generations is based on FTDNATiP™ Reports, Most Recent Common Ancestor Time Predictor based on Y-STR Genetic Distance

Understanding Y-DNA Genetic Distance, FTDNA Help Center, https://help.familytreedna.com/hc/en-us/articles/6019925167631-Understanding-Y-DNA-Genetic-Distance

Concepts – Genetic Distance, DNAeXplained – Genetic Genealogy,, Blog, 29 June 2016, https://dna-explained.com/2016/06/29/concepts-genetic-distance/

[13] J David Vance, The Genealogist Guide to Genetic Testing, 2020 , Chapter 5, https://www.amazon.com/Genealogists-Guide-Testing-Genetic-Genealogy/dp/B085HQXF4Z/ref=tmm_pap_swatch_0?_encoding=UTF8&qid=&sr=

[14] Ibid.

[15] These illustrations of the relationship between genetic distance and generations are from: David Vance, The Genealogist Guide to Genetic Testing, 2020 , Chapter 5

The statistical analyses were based on:

J. Douglas McDonald, TMRCA Calculator, Oct 2014 version, Clan Donald, USA website, Https://clandonaldusa.org/index.php/tmrca-calculator

[16] “For the Y chromosome these rates assume a 31 year generation.”

J. Douglas McDonald, TMRCA Calculator, Oct 2014 version, Clan Donald, USA website, Https://clandonaldusa.org/index.php/tmrca-calculator

[17] “The original FTDNATiP™ Report was based on research by Bruce Walsh, Professor at the University of Arizona, and his 2001 paper in Genetics. Walsh used a theoretical approach to model STR mutation rates and estimate when two people’s’ paths diverged in the Y-DNA haplotree. He used an infinite allele model, which theoretically accounts for markers mutating more than once, which can obscure the true mutation rate.”

Introducing the New FTDNATiP™ Report for Y-STRs, FTDNA Blog, 16 Feb 2023, https://blog.familytreedna.com/ftdnatip-report/

[18] Big Y Age Estimates: Updates and the Battle of Falkirk, FTDNA Blog, 9 Sep 2022, https://blog.familytreedna.com/tmrca-age-estimates-update/

Phylogenetic age estimation, otherwise known as “divergence dating,” has a long and rich history that began in the 1960s. Two general classes of methods have emerged: a strict molecular clock, and a relaxed clock. Sep 19, 2022, FTDNA Blog, https://blog.familytreedna.com/tmrca-age-estimates-scientific-details/

The Group Time Tree: A New Big Y Tool for FamilyTreeDNA Group Projects, FamilyTreeDNA Blog, 15 Feb 2023, https://blog.familytreedna.com/group-time-tree/

[19] Introducing the New FTDNATiP™ Report for Y-STRs, FTDNA Blog, 16 Feb 2023, https://blog.familytreedna.com/ftdnatip-report/

[20] David Vance, The Life of Trees   (Or:  Still Another Phylogeny Program),SAPP Tree Generator V4.25, http://www.jdvsite.com

Dave Vance, Y-DNA Phylogeny Reconstruction using likelihood-weighted phenetic and cladistic data – the SAPP Program, 2019, academia.edu, https://www.academia.edu/38515225/Y-DNA_Phylogeny_Reconstruction_using_likelihood-weighted_phenetic_and_cladistic_data_-_the_SAPP_Program

Y-DNA tools, International Society of Genetic Genealology Wiki, This page was last edited on 30 June 2022,   https://isogg.org/wiki/Y-DNA_tools

Sennet Family Tree Blog, The SAPP is up and running: a phylogenetic analysis of Sennett surname project members, 8 May 2021, https://sennettfamilytree.wordpress.com/2021/05/08/the-sapp-is-up-and-running-a-phylogenetic-analysis-of-sennett-surname-project-members/

[21] Introduction to Distance Dendrograms, Tracking Back: A Website for Genetic Genealology Tools, experimentation, and discussion, http://scaledinnovation.com/gg/gg.html?rr=ddintro

Michael Drout and Leah Smith, How to read a Dedrogram, Wheaton college, https://wheatoncollege.edu/wp-content/uploads/2012/08/How-to-Read-a-Dendrogram-Web-Ready.pdf

Tim Bock, What is a Dendrogram, DisplayR blog, no date, https://www.displayr.com/what-is-dendrogram/

Dendrograpm, Wikipedia, page was last edited on 7 September 2022  , https://en.wikipedia.org/wiki/Dendrogram

Prasad Pai Hierarchical clustering explained, Towards Data Science, 7 May 2021, https://towardsdatascience.com/hierarchical-clustering-explained-e59b13846da8

Tom Tullis, Bill Albert, Hierarchical Cluster Analysis,  in Measuring the User Experience (Second Edition), 2013  https://www.sciencedirect.com/topics/computer-science/hierarchical-cluster-analysis

Rob Spencer, Simple Distance Tree, Tracking Back – a website for genetic genealogy tools, experimentation, and discussion, 2023-01-28, ,http://scaledinnovation.com/gg/treeDemo.html

Rob Spencer, Family Tree and Y-DNA Simulator, Tracking Back – a website for genetic genealogy tools, experimentation, and discussion, http://scaledinnovation.com/gg/familySimulator.html

[22] Rob Spencer, Y STR Clustering and Dendrogram Drawing, Click on Discussion Tab, Tracking Back Click – a website for genetic genealogy tools, experimentation, and discussion, http://scaledinnovation.com/gg/clustering.html

[23] Introduction to Distance Dendrograms, Tracking Back: A Website for Genetic Genealology Tools, experimentation, and discussion, http://scaledinnovation.com/gg/gg.html?rr=ddintro

[24] Rob Spencer, The Big Picture of Y STR Patterns, The 14th International Conference on Genetic Genealogy, Houston, TX March 22-24, 2019,  http://scaledinnovation.com/gg/ext/RWS-Houston-2019-WideAngleView.pdf Page 28

[25].Rob Spencer, Introduction to Distance Dendrograms, Tracking Back: A Website for Genetic Genealology Tools, experimentation, and discussion, http://scaledinnovation.com/gg/gg.html?rr=ddintro

[26] Rob Spencer, The Big Picture of Y STR Patterns, The 14th International Conference on Genetic Genealogy, Houston, TX March 22-24, 2019,  http://scaledinnovation.com/gg/ext/RWS-Houston-2019-WideAngleView.pdf

[27] Rob Spencer, The Big Picture of Y STR Patterns, The 14th International Conference on Genetic Genealogy, Houston, TX March 22-24, 2019,  http://scaledinnovation.com/gg/ext/RWS-Houston-2019-WideAngleView.pdf Page 12

Source: Rob Spencer Click for Larger View

[28] Rob Spencer, The Big Picture of Y STR Patterns, The 14th International Conference on Genetic Genealogy, Houston, TX March 22-24, 2019,  http://scaledinnovation.com/gg/ext/RWS-Houston-2019-WideAngleView.pdf Page 11

Source: Rob Spencer Click for Larger View