{{Rsnum
|rsid=10476160
|Chromosome=5
|position=175547573
|Orientation=plus
|GMAF=0.3173
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 72.6 | 24.8 | 2.7
| HCB | 54.1 | 36.3 | 9.6
| JPT | 52.2 | 39.8 | 8.0
| YRI | 13.6 | 53.1 | 33.3
| ASW | 28.1 | 47.4 | 24.6
| CHB | 54.1 | 36.3 | 9.6
| CHD | 62.4 | 30.3 | 7.3
| GIH | 70.3 | 27.7 | 2.0
| LWK | 10.2 | 47.2 | 42.6
| MEX | 50.0 | 44.8 | 5.2
| MKK | 21.2 | 55.1 | 23.7
| TSI | 52.0 | 40.2 | 7.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=
  |Pval=9E-9
  |OR=1.61
  |ORtxt=[NR]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}