{{Rsnum
|rsid=17119461
|Chromosome=10
|position=107516352
|Orientation=plus
|GMAF=0.07117
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.9 | 1.8 | 97.3
| HCB | 0.0 | 9.5 | 90.5
| JPT | 0.0 | 3.5 | 96.5
| YRI | 8.2 | 36.1 | 55.8
| ASW | 3.5 | 35.1 | 61.4
| CHB | 0.0 | 9.5 | 90.5
| CHD | 0.0 | 7.3 | 92.7
| GIH | 1.0 | 16.8 | 82.2
| LWK | 5.5 | 35.5 | 59.1
| MEX | 0.0 | 8.6 | 91.4
| MKK | 3.8 | 38.5 | 57.7
| TSI | 0.0 | 3.0 | 97.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21706340
|Trait=None
|Title=A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.
|RiskAllele=
|Pval=7E-12
|OR=8.4000
|ORtxt=[4.20-17.0]
}}

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