R L21, Z290 and Subclades

If R-L21, R-DF13 or any subclade of R-Z290 - JOIN >>>>
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About us

Welcome to the R1b-L21 & R1b-Z290 and Subclades Project!

R1b-L21 is the branch of the human family tree marked by the mutation L21+. This includes all R-L21 people. It is the most common Y chromosome subclade of paternal lineages in the British Isles and is also significant in France. It is found across Western and Central Europe as well as Scandinavia. Other names for L21+ are M529+, S145+. Other SNPs that are equivalent to L21+ are L459+, FGC3218+. Recently we've discovered that Z245, Z260 and Z290 are equivalent to each other but slightly older than L21 so Z290+ people are also included. There are over 1,700 branches and over 6,000 SNPs on FTDNA's R1b-L21 haplotree. The larger subclades are marked by CTS4466+, DF13+, DF21+, DF41+, DF49+, DF63+, FGC5494+, L1335+, L513+, S1026+, S1051+, M222+, Z251+, Z253+, Z255+, Z2542+. If you are positive for any of SNPs listed or any other descendant SNP, you are invited to join the project. Just click on the JOIN button above in the banner and login in with your kit #.

The goals of the R1b-L21 & R1b-Z290 and Subclades project are to gain deeper understanding of the origins and migrations of our male lineages, as R1b-L21 people, while helping you find family paternal lineages and deep ancestral origins. An important role of the project is to support DNA testing steps that will help identify where you fit within R1b-L21. This may lead you to one of the large subclade of L21 projects, which are highly recommended.

Even if you are engaged in other projects and are already deeply tested, please join or to continue in the R1b-L21 & Z290 project, but in the role as a model for others. We need people who have tested deeply to stay in the project and be included in the R1b-L21 Haplotypes comparisons so the new people can learn what testing they might consider and the compare themselves with model haplotype results. Leaders want potential matches to find them and test for their SNPs as documented on the tree. The best models are those with Big Y and 111 STR tests completed. We also need thought and discussion leadership.

An important task is to discover the full deep ancestral family tree of paternal lineages for all R1b-L21 people. This will help us understand the origins of R1b-L21 as a whole, at the subclade levels and down to the genealogical family tree level. The primary method of marking branches in the tree are SNPs so this project is for people who are interested in SNP testing.  Please read this web page entirely. Below you will find:

Key Steps to Take

Project Considerations and Operations

More about SNPs

Key Steps to Take 

1. You must have a Y DNA test result and at least 12 Y STRs with Family Tree DNA (FTDNA.) National Genographic Project testers can easily join, but first you must transfer your test results to FTDNA by following the instructions at your National Genographic web page. Testers will not appear on the project screens and in the Y matching system without the STRs.

2. To join this project click on JOIN in the graphic banner above and login with your FTDNA account ID and password.

3. Update your myFTDNA dashboard by clicking on MANAGER PERSONAL INFORMATION. This is critical to finding potential relatives and understanding origins.

3A. Make sure your privacy settings are correct for the project. Click on the tab PRIVACY & SHARING. Look under MY DNA RESULTS for the question "Who can view my DNA results in group projects?".  Change to ANYONE if not already.

3B. Update your Paternal Ancestor name and origins. Click on the tab PERSONAL PROFILE tab and scroll down to update your paternal origins information from the MyFTDNA dashboard after logged into. Select MOST DISTANT ANCESTORS and complete the information for your PATERNAL DIRECT most distant (oldest) ancestor. Please enter only information that is not speculative. Enter first and last names, birth year and as specific a birth and origin location as you can in the NAME field. For example, “James Welch, b.c.1812, Co. Kilkenny, Ireland”. For the COUNTRY OF ORIGIN field, please be as specific as possible. For instance, rather than select UNITED KINGDOM please pick either ENGLAND, IRELAND, NORTHERN IRELAND, SCOTLAND OR WALES if you know the origin. Add the latitude and longitude information as well so that the automatic maps can be drawn properly.
If you don't know, that is okay. Unknown may be the best answer.

4. Join the Yahoo discussion group for this project. Several project administrators and advanced R1b-L21 hobbyists are available on the R1b-L21-project yahoo forum so you can get help and share ideas. There are also links to scientific papers, research data, etc. on this group. You can use a nickname rather than your actual name for this forum. You can email R1b-L21-project-subscribe@yahoogroups.com to subscribe or visit http://groups.yahoo.com/neo/groups/R1b-L21-project/info

5. If you have not yet tested to 111 Y STRs (Short Tandem Repeats) please upgrade. R1b is young so it is hard to discern between subgroups and potential relatives oftentimes without 67 STRs as a bare minimum. 111 STR testing is clearly preferable and a better deal in terms of cost per STR. To learn more, read http://www.familytreedna.com/learn/y-dna-testing/y-str/upgrading-markers-improve-information/

More STRs can help...
a) identify your signature markers, guiding you on SNP/haplogroup testing and saving money on that kind of testing,
b) provide additional and better matches on your myFTDNA matches screen, even new matches can show up,
c) improve precision for Time to Most Recent Common Ancestor (TMRCA) estimates,
d) and going all the way to 111 Y STRs supports family tree building when you reach brick walls in your genealogy, since the 111 STR panel is estimated to have a change once every three generations.

6. Move forward with an Single-Nucleotide Polymorphism (SNP) testing plan so your subclade can be identified and haplogroup labeled properly. Evaluating matches you have at 67 or 111 STRs can be very helpful and should not be overlooked. Clear patterns among your best matches may help you decide what SNPs or SNP Packs to buy.

SNPs can be ordered one at a time from FTDNA by logging into your myFTDNA account, selecting the blue UPGRADES button and then scrolling down to the ADVANCED TESTS box and the BUY NOW button. SNP Packs can also be ordered here.

6A. Big Y is the preferred test.  It is probably the most important test you can take. It is a Next Generation Sequencing (NGS) test that discovers new SNPs by scanning over 10 million locations on the Y chromosome. The tremendous benefit in this is you will discover SNPs for just your paternal lineage as well as identify ancient SNPs that you may share with many, many other people. Big Y has the ability to discover SNPs that are pertinent to the genealogical timeframe, the last couple of hundred years. The Big Y learning web site has more details. http://www.familytreedna.com/learn/y-dna-testing/big-y/ Please read the Lewis and Clark Expedition analogy for Big Y exploration on the R1b project FAQ page. http://www.familytreedna.com/groups/r-1b/faq/

6B. The R1b-L21 SNP Pack is a very cost effective option that provides very good coverage of the early branching and smaller subclades of R1b-L21. It can place you in the appropriate major subclades of R1b-L21. You can order it from your myFTDNA account. If you don't see the option, please check the blue UPGRADES button, then the BUY NOW button in the ADVANCED TESTS box, and pick SNP PACK in the SELECT A PRODUCT box. See the R-L21 project FAQ web page for a list of packs and guidance. Please post on the R1b-L21-project yahoo group if you have questions.

If you have a true interest in genetic genealogy and breaking beyond the brickwalls of your genealogical records, please strongly consider both Big Y to determine your haplogroup down to a very recent timeframe and 111 STRs so that you can refine your close-in family and surname mutation history tree.

Project Considerations and Operations

The project administrators are volunteers and do not represent the vendors nor receive special benefits.

This is a public project. The more of us who test and share our information, the more we will all know. When you join this project, you are granting permission to place your Y SNP and STR data into the public domain, from which it can never be retrieved. We do not publish your full given name or contact info.

This is a Y DNA haplogroup project. Actively participating involves Y SNP testing. SNP testing is required to be assigned to a subgrouping.

This project is operated as a system of record project. It is intended to operate for posterity purposes. Our descendants and family members and distant cousins can continue on when we are not able to or have new focuses in life. New generations can build upon our work. Subgroupings are done by SNP validated testing with a chain of evidence to the test results. Surnames and STR based predictions are not used to assigned subgroupings. SNP results researched without FTDNA test validation are not included so please validate findings with FTDNA testing. Outside research is good, but please validate branching at FTDNA for the project test results. As changes are made to project administrators the subgroupings can be reconstructed or re-validated as needed given they are based on test results on the Y DNA SNP report page of the project.

The project is designed to support genetic genealogy for hobbyists. It is not intended for forensic or legal purposes. FTDNA policies apply.

Thank you for your consideration. Please review the Results web page. If you have specific questions please post join the R1b-YDNA discussion group at http://groups.yahoo.com/neo/groups/R1b-L21-project/info

More about SNPs

Single-Nucleotide Polymorphisms (SNPs) are critical for R1b people as they are very stable, rarely mutating. R1b is both a very large group and relatively young. Most European R1b paternal lineages are related within the last several thousand years. That means that R1b STR based haplotypes often look alike. The most common pattern of Y STRs is the Western Atlantic Modal Haplotype (WAMH). Most R1b people match several components of it. It is just a remnant of the fact we are closely related. SNPs help differentiate the branches of R1b-L21’s descendants tree. A high level simplified version is on this project's About Overview web page.

R1b-L21 itself, the main branch of our tree, is marked by the SNP L21. We all are L21+ since it was present in our common ancestor, a single prehistoric man. There are now thousands of known branches on the R1b tree.

Many of these branches have coincidentally matching Y STRs. In other words, their branches appear to cross. This gives us false matches.This is definitely a problem with limited haplotypes of 37 or less STRs. 67 is really the bare minimum in most cases and 111 is the new standard. There are now 6,000-10,000 L21 people with 111 STRs in FTDNA's database.

STRs are very useful for general guidance and for matching at the very recent family level, but they are not 100% reliable since some mutate relatively quickly and go both up and down and back to where they started from.

SNPs are much more reliable markers for our paternal lineages. Theoretically, they are permanent throughout eternity so they reliably show our branching of paternal lineages. The number of SNPs available for testing is growing as more and more advanced testing is developed. You will want to identify your terminal SNP, which is the youngest SNP mutation that you have, that is on a formal Y DNA tree. Your terminal SNP tells you where you fit from a deep ancestral perspective.

SNPs help...
a) make you more efficient by avoiding false matches when checking for potential genealogical relationships,
b) help you identify deep ancestral family, clan or historical origins,
c) show you what geographic locations might produce additional matches and pertinent genealogical or historical information and
d) benefit all R1b people in general, as well as science, because we'll have a better understanding of how and when this lineage of men spread across Europe as rapidly and as dominantly as it did.

For additional information on SNP testing please visit http://dna-explained.com/2012/08/10/to-snp-or-not-to-snp/

Frequently Asked Questions are answered on the R1b FAQ page

Why Y DNA testing?

Why DNA testing at a full platform genetic genealogy company?

Why Y STRs and how are they used?

Why Y SNPs and how are they used?

Why Big Y Next Generation Sequencing?

Should I upgrade Y STRs, even if I have limited or no matches?

What are SNP Packs and which should I consider?

What are terminal SNPs? novel SNPs? private and public SNPs?

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