{{Rsnum
|rsid=1417210
|Chromosome=10
|position=73135919
|Orientation=minus
|GMAF=0.1768
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 1.8 | 20.4 | 77.9
| HCB | 9.5 | 46.7 | 43.8
| JPT | 15.9 | 41.6 | 42.5
| YRI | 0.0 | 2.7 | 97.3
| ASW | 0.0 | 3.5 | 96.5
| CHB | 9.5 | 46.7 | 43.8
| CHD | 12.0 | 31.5 | 56.5
| GIH | 2.0 | 37.6 | 60.4
| LWK | 0.0 | 7.3 | 92.7
| MEX | 10.3 | 44.8 | 44.8
| MKK | 0.6 | 7.7 | 91.7
| TSI | 1.0 | 22.5 | 76.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22951725
  |Trait=Vitiligo
  |Title=Association analyses identify three susceptibility Loci for vitiligo in the Chinese Han population.
  |RiskAllele=
  |Pval=2E-8
  |OR=1.14
  |ORtxt=[1.09-1.19]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}