{{Rsnum
|rsid=1985317
|Chromosome=9
|position=117530056
|Orientation=minus
|GMAF=0.4004
|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 | 33.0 | 50.0 | 17.0
| HCB | 5.8 | 32.8 | 61.3
| JPT | 7.1 | 39.8 | 53.1
| YRI | 3.4 | 31.5 | 65.1
| ASW | 7.0 | 43.9 | 49.1
| CHB | 5.8 | 32.8 | 61.3
| CHD | 4.6 | 36.7 | 58.7
| GIH | 26.7 | 44.6 | 28.7
| LWK | 5.6 | 38.3 | 56.1
| MEX | 5.4 | 57.1 | 37.5
| MKK | 9.6 | 44.9 | 45.5
| TSI | 23.8 | 64.4 | 11.9
| 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=1E-9
  |OR=1.52
  |ORtxt=[NR]
  |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}}