rs11799226

A SNP on chromosome Y. Its most notable genotype is G;G: L21+

Gene
None listed
Location
Chr Y13,542,548 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
3%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableNot ratedL21+Typical · 0.0

On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Genosets

Genosets combine several genotypes. Twofold checks them in your report.

Notes

From SNPedia

Show notes, about 130 words

23andMe discussion R1b large group splits for rs11799226 ; C is ancestral and G is derived . if you have G, please show up and sign here (geographical origin is welcome). http://www.familytreedna.com/public/R-L21/default.aspx ==Associated Genosets== {| class="wikitable sortable" |+ Haplogroup R1b1b2a1a2f and Subclades |- ! Haplogroup ! Parent Haplogroup ! Publication ! Defining SNPs ! 23andMe Genoset ! deCodeMe Genoset ! Full Genomic Sequence (FTDNA and Argus Bio) |- |R1b1b2a1a2f1 ||R1b1b2a1a2f || || M37 (private, 23andMe) || || || |- |R1b1b2a1a2f2 ||R1b1b2a1a2f || || M222/USP9Y+3636 || gs214 || || |- |R1b1b2a1a2f3 ||R1b1b2a1a2f || || P66 (private) || || || |- |R1b1b2a1a2f4 ||R1b1b2a1a2f || || L226/S168 || || || |- |R1b1b2a1a2f5 ||R1b1b2a1a2f || || L193/S176 || || || |}

Source and license

Adapted from rs11799226 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.