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.

  1. A;AMost notableGoodnormalTypical · 0.036% of people
  2. A;GBad1.18x risk of vitiligo in ChineseTypical · 0.038% of people
  3. G;GBad1.18x risk of vitiligo in ChineseTypical · 0.026% of people

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%

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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.