{{Rsnum
|rsid=673604
|Chromosome=1
|position=35222214
|Orientation=plus
|GMAF=0.3985
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 21.2 | 78.8
| HCB | 37.3 | 54.5 | 8.2
| JPT | 36.9 | 51.4 | 11.7
| YRI | 37.5 | 47.9 | 14.6
| ASW | 37.5 | 39.3 | 23.2
| CHB | 37.3 | 54.5 | 8.2
| CHD | 36.4 | 44.9 | 18.7
| GIH | 6.0 | 31.0 | 63.0
| LWK | 41.7 | 45.4 | 13.0
| MEX | 12.3 | 47.4 | 40.4
| MKK | 30.8 | 42.3 | 26.9
| TSI | 0.0 | 12.7 | 87.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21499250
|Trait=None
|Title=Genome-wide association study identifies a common variant associated with risk of endometrial cancer.
|RiskAllele=
|Pval=0.000006
|OR=1.2100
|ORtxt=[1.12-1.32]
|OA=1
}}

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