{{Rsnum
|rsid=2282015
|Chromosome=10
|position=125222037
|Orientation=minus
|GMAF=0.4261
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 46.0 | 35.4 | 18.6
| HCB | 27.9 | 50.0 | 22.1
| JPT | 20.4 | 52.2 | 27.4
| YRI | 46.3 | 40.1 | 13.6
| ASW | 52.6 | 40.4 | 7.0
| CHB | 27.9 | 50.0 | 22.1
| CHD | 28.4 | 50.5 | 21.1
| GIH | 56.4 | 39.6 | 4.0
| LWK | 34.5 | 50.0 | 15.5
| MEX | 22.4 | 67.2 | 10.3
| MKK | 23.2 | 50.3 | 26.5
| TSI | 28.4 | 50.0 | 21.6
| 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=8E-10
  |OR=1.50
  |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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}