rs10876864
A SNP in the SUOX gene on chromosome 12. Its most notable genotype is A;A: normal
- Gene
- SUOX
- Location
- Chr 1256,007,301 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 45%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableGoodnormal
- A;GBad1.18x risk of vitiligo in Chinese
- G;GBad1.18x risk of vitiligo in Chinese
On SNPedia: (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.
- AverageA;A 36% A;G 38% G;G 26%
- European ancestry (Utah)A;A 36% A;G 47% G;G 17%
- Han Chinese (Beijing)A;A 58% A;G 36% G;G 7%
- Japanese (Tokyo)A;A 58% A;G 41% G;G 2%
- Yoruba (Nigeria)A;A 3% A;G 23% G;G 75%
- African ancestry (Southwest US)A;A 7% A;G 39% G;G 54%
- Chinese (Denver)A;A 60% A;G 34% G;G 6%
- Gujarati IndianA;A 59% A;G 32% G;G 9%
- Luhya (Kenya)A;A 4% A;G 28% G;G 68%
- Mexican ancestry (Los Angeles)A;A 55% A;G 36% G;G 9%
- Maasai (Kenya)A;A 17% A;G 51% G;G 32%
- TuscanA;A 38% A;G 52% G;G 11%
Related
Source and license
Adapted from rs10876864 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.