rs1268524
A SNP in the SLAMF6 gene on chromosome 1. Its most notable genotype is C;T.
- Gene
- SLAMF6
- Location
- Chr 1160,500,468 (GRCh38)
- Highest magnitude
- 0.2Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 30%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TNot ratedNo summary available.
- C;TMost notableNot ratedNo summary available.
- C;CNot ratedNo summary available.
SNPedia records rs1268524 on the minus strand: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageT;T 49% C;T 41% C;C 10%
- European ancestry (Utah)T;T 55% C;T 39% C;C 6%
- Han Chinese (Beijing)T;T 47% C;T 46% C;C 7%
- Japanese (Tokyo)T;T 51% C;T 43% C;C 6%
- Yoruba (Nigeria)T;T 68% C;T 27% C;C 5%
- African ancestry (Southwest US)T;T 61% C;T 30% C;C 9%
- Chinese (Denver)T;T 51% C;T 41% C;C 7%
- Gujarati IndianT;T 37% C;T 46% C;C 18%
- Luhya (Kenya)T;T 49% C;T 42% C;C 9%
- Mexican ancestry (Los Angeles)T;T 45% C;T 47% C;C 9%
- Maasai (Kenya)T;T 35% C;T 46% C;C 19%
- TuscanT;T 42% C;T 45% C;C 13%
Related
Notes
From SNPedia
Notes
flanking snp for a region related to deafness
Source and license
Adapted from rs1268524 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.