rs2506933
A SNP on chromosome 6. Its most notable genotype is T;T: common in complete genomics
- Gene
- None listed
- Location
- Chr 692,905,732 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 24%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (T;T). 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 55%
- European ancestry (Utah)T;T 91%
- Han Chinese (Beijing)T;T 71%
- Japanese (Tokyo)T;T 78%
- Yoruba (Nigeria)T;T 10%
- African ancestry (Southwest US)T;T 23%
- Chinese (Denver)T;T 77%
- Gujarati IndianT;T 76%
- Luhya (Kenya)T;T 17%
- Mexican ancestry (Los Angeles)T;T 43%
- Maasai (Kenya)T;T 24%
- TuscanT;T 91%
Notes
From SNPedia
Notes
non sig. gwas, hit (p = 6 x 10^-6) - Animals
Source and license
Adapted from rs2506933 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.