{{Rsnum
|rsid=493014
|Chromosome=9
|position=133320327
|Orientation=plus
|GMAF=0.3095
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 15.9 | 42.5 | 41.6
| HCB | 0.0 | 17.5 | 82.5
| JPT | 0.0 | 18.6 | 81.4
| YRI | 44.2 | 44.2 | 11.6
| ASW | 31.6 | 49.1 | 19.3
| CHB | 0.0 | 17.5 | 82.5
| CHD | 0.0 | 15.6 | 84.4
| GIH | 7.9 | 40.6 | 51.5
| LWK | 32.7 | 46.4 | 20.9
| MEX | 1.7 | 29.3 | 69.0
| MKK | 33.3 | 42.3 | 24.4
| TSI | 8.8 | 39.2 | 52.0
| 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=A
  |Pval=6E-11
  |OR=1.64
  |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}}