{{Rsnum
|rsid=2028385
|Chromosome=12
|position=96423644
|Orientation=plus
|GMAF=0.2296
|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 | 70.5 | 26.8 | 2.7
| HCB | 61.3 | 31.4 | 7.3
| JPT | 52.2 | 38.1 | 9.7
| YRI | 47.3 | 45.9 | 6.8
| ASW | 54.4 | 40.4 | 5.3
| CHB | 61.3 | 31.4 | 7.3
| CHD | 53.3 | 39.0 | 7.6
| GIH | 61.4 | 34.7 | 4.0
| LWK | 38.2 | 46.4 | 15.5
| MEX | 0.0 | 0.0 | 0.0
| MKK | 47.1 | 44.4 | 8.5
| TSI | 67.6 | 28.4 | 3.9
| 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=C
  |Pval=9E-9
  |OR=1.69
  |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}}