rs1417210

A SNP on chromosome 10. Its most notable genotype is G;G: 0.88x risk of vitiligo in Chinese

Gene: None listed
Location: Chr 1071,376,162 (GRCh38)
Highest magnitude: 0.0Typical
Tested on: 23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency: 18%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

SNPedia records rs1417210 on the minus strand: (C;C), (C;T), (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.

AverageG;G 5% A;G 24% A;A 71%
European ancestry (Utah)G;G 2% A;G 20% A;A 78%
Han Chinese (Beijing)G;G 10% A;G 47% A;A 44%
Japanese (Tokyo)G;G 16% A;G 42% A;A 43%
Yoruba (Nigeria)G;G 0% A;G 3% A;A 97%
African ancestry (Southwest US)G;G 0% A;G 4% A;A 97%
Chinese (Denver)G;G 12% A;G 32% A;A 57%
Gujarati IndianG;G 2% A;G 38% A;A 60%
Luhya (Kenya)G;G 0% A;G 7% A;A 93%
Mexican ancestry (Los Angeles)G;G 10% A;G 45% A;A 45%
Maasai (Kenya)G;G <1% A;G 8% A;A 92%
TuscanG;G 1% A;G 23% A;A 77%

Source and license

Adapted from rs1417210 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.