{{Rsnum
|rsid=318497
|Chromosome=6
|position=2912043
|Orientation=plus
|GMAF=0.4793
|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 | 21.2 | 50.4 | 28.3
| HCB | 34.1 | 50.4 | 15.6
| JPT | 34.2 | 47.7 | 18.0
| YRI | 19.0 | 51.0 | 29.9
| ASW | 21.1 | 43.9 | 35.1
| CHB | 34.1 | 50.4 | 15.6
| CHD | 22.2 | 52.8 | 25.0
| GIH | 12.9 | 48.5 | 38.6
| LWK | 8.3 | 47.2 | 44.4
| MEX | 33.9 | 44.6 | 21.4
| MKK | 14.7 | 44.2 | 41.0
| TSI | 22.8 | 50.5 | 26.7
| 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=5E-9
  |OR=2.33
  |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}}