Relative Finder is an opt-in feature of the personal genome service offered by 23andMe. It can be accessed from the "My Ancestry" Menu in the 23andMe user interface. It was beta-tested by members of the genetic genealogy community during fourth quarter 2009 and entered a public beta-test on November 9, 2009. It was released to the general public first quarter 2010.
Relative Finder uses Autosomal DNA to help find relatives from all parts of one's family tree. Until recently, DNA genealogy tests could only tell a person about a small part of their family tree, because they only used DNA from the Y chromosome and mitochondria. By using Autosomal DNA (abbreviated as atDNA), Relative Finder can trace any ancestral line, no matter where it is in the family tree.
The science behind the feature involves comparing the atDNA of all participants to discover matching DNA segments equal to or greater than seven Centimorgans (abbreviated as cMs) on one segment, and if met, five cMs on the rest with 700 or more SNPs. The participant is then provided with an anonymous list of predicted relatives. The participant can send a message via 23andMe to his or her matches, but is restricted to sending five messages per day. It is therefore best to focus initially on the closest matches and the matches who have indicated that they have listed a large number of surnames on their profile page.
Relative Finder is available to customers who purchase the Ancestry Edition or Complete Edition.
Steps to find your common ancestor for matches at 23andMe
When you receive a match in Relative Finder, the first thing you must consider is the Predicted Relationship, as well as the Relationship Range. This gives you what the company feels your possible relationship is, with the Relationship Range giving you a range of where the actual relationship may be. Understand that relationships can also be outside of this range, as well, as testing autosomal DNA is not an exact science due to recombination. Also listed is the % of Shared DNA and # of Shared Segments.
The next step is to decide who to contact from your list. A good place to start is by contacting those who have the closest relationship to you. From the Relative Finder screen you can use the Make Contact button to send a message to your match(es) and request to share genomes at the Basic Level. Once your match agrees, next go to Family Inheritance: Advance under Ancestry Labs in the left hand column of your screen. Once on the screen, select the person in question to compare.
Select View in a Table and you will see the following information:
|| Start Point-End Point
|| Genetic Distance
|| # SNPs|
| Jim Jones vs Sally Lee
|| 19000000 - 133000000
|| 28.5 cM
Look at the Genetic Distance column to determine the longest block of Centimorgans (cMs) listed for the match. Once you determine the longest block of cMs, the following Match Outcomes list should give you an idea of where your actual relationship may lie and where in your family tree to look.
- 10 cMs or higher indicates a match usually within 5 generations (4th or more recent cousins)* - better chance to find a match with a highly developed genealogy
- 5-9 cMs can cover a range of 6 to 11 generations (5th to distant cousins)* – later generations may include low level matches that show you probably share a common ancestor but may not be able to effectively trace genealogically
- Below 5 cMs (Mb) gives ancient ancestry
A generation can run an average of every 25–35 years. To understand generations and cousinship levels, check the following chart courtesy of Family Tree DNA FAQ.
Why would my parent match someone and I don’t?
There is a 50-50 chance of inheriting the chromosome that contains the match (as opposed to a smaller chance of a small segment being broken up into still smaller segments). In other words, if your mother's match came from her mother's side of the family, she must have given you the portion that came from her father's side instead. If you look at the Family Inheritance diagrams at 23andMe for the demo Mendel family, you can see that the three grandchildren have matching segments with their maternal grandmother OR their maternal grandfather, never both. Take Ian Mendel, for example, and switch back and forth between comparisons with his maternal grandparents, Ron and Margo Fisher. It's like looking at a photo and its negative.
Why do three people from different generations all have the same-sized segment?
One person had this situation: "On Chromosome 10: I match exactly, the father, his daughter and his granddaughter: Same segment, same cM, same number SNPs (0.10%). Relative Finder lists all three as 4th to 10th cousins. I had expected to see a (declining size/SNP count), from the father to granddaughter."
Yes, that's an illustration of the 50-50 random chance. When you get down to a small segment, the probability is actually higher that you will inherit all of it (in this case) or none of it (as in the first case listed above), vs a recombination event that happens to occur right smack dab in the middle of it and chops it into even smaller pieces. The shorter chromosomes typically have just one cross-over point, while the longer ones may have two cross-over points. (From a message from Ann Turner on the ISOGG mailing list.)
On August 14, 2010, 23andMe added the ability to download a csv file of all Relative Finder matches. This option is located in the top right corner of the list of Relative Finder matches.
On July 22, 2010, 23andMe added the ability for each customer to choose to make his/her profile a Relative Finder "Public Match". These public profiles will automatically be shown on Relative Finder and Ancestry Finder Lab when a match is found with another customer. This eliminates the need for an invitation to be sent to these public profiles and allows their matches to explore their profiles immediately.
To choose to be a "Public Match" follow these steps:
1. Log in to your 23andMe account
2. Go to the top right of the screen and select "Account"
3. From the drop down menu go to "Settings"
4. Go to the "Privacy/Consent" page
5. On the "Privacy/Consent" page, check the box that says "I want to make my profile publicly visible in Relative Finder and the Ancestry Finder Lab."
- Please note - If there are multiple profiles in the account, this must be done separately for each one.
X chromosome matches
Thresholds for relationship matches
Initially, the information provided by 23andMe referred to matching DNA segments equal to or greater than seven cM on one segment, and if met, five cMs on the additional segments, all with 700 or more SNPs. Later they happened to mention that the above applied to autosomes, but X chromosome thresholds are quite different, and gender-specific. Still later, error thresholds were mentioned. For Relative Finder (but not for Ancestry Finder) at least one segment must equal or exceed 7 cM.
- For half-IBD segments, the thresholds are:
autosomal: 700 SNPs, 5 cM
X (male vs male): 200 SNPs, 1 cM
X (male vs female): 600 SNPs, 6 cM
X (female vs female): 1200 SNPs, 6 cM
The maximum amount of error tolerated in a half-IBD segment would be roughly 1 opposite homozygote per 300 SNPs; furthermore, each such opposite homozygote in a half-IBD segment must be separated by roughly 300 SNPs (i.e., the length of a sub-segment).
- For full-IBD segments, the thresholds are:
autosomal and X: 500 SNPs, 5 cM.
The criteria roughly correspond to allowing an error rate of 1%.
- Family Finder versus Relative Finder
- Ancestry Finder
- Family Inheritance: Advanced
- Ancestry Painting
- Native American Ancestry Finder
- Compare Genes
- 23andMe Relative Finder offical site
- What's the average % DNA shared for different types of cousins 23andMe FAQ
- X Marks the Spot -thread with threshold details. (Access is restricted to customers.)
- Great-Grandparent Inheritance Your Genetic Genealogist Blog
- "Hey Bro" Relative Finder DNA adoption success story on 23andMe's "The Spittoon"