{{Rsnum
|rsid=971572
|Chromosome=1
|position=184099374
|Orientation=minus
|GMAF=0.3549
|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 | 37.2 | 48.7 | 14.2
| HCB | 21.3 | 45.6 | 33.1
| JPT | 14.2 | 54.0 | 31.9
| YRI | 83.6 | 15.1 | 1.4
| ASW | 64.9 | 31.6 | 3.5
| CHB | 21.3 | 45.6 | 33.1
| CHD | 17.6 | 44.4 | 38.0
| GIH | 29.7 | 49.5 | 20.8
| LWK | 74.3 | 24.8 | 0.9
| MEX | 38.6 | 47.4 | 14.0
| MKK | 72.9 | 27.1 | 0.0
| TSI | 52.9 | 39.2 | 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=2.38
  |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}}