{{Rsnum
|rsid=1423386
|Chromosome=5
|position=62689026
|Orientation=minus
|GMAF=0.2287
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 1.8 | 25.9 | 72.3
| HCB | 11.7 | 47.4 | 40.9
| JPT | 10.6 | 39.8 | 49.6
| YRI | 5.4 | 33.3 | 61.2
| ASW | 1.8 | 28.1 | 70.2
| CHB | 11.7 | 47.4 | 40.9
| CHD | 12.0 | 50.0 | 38.0
| GIH | 1.0 | 23.8 | 75.2
| LWK | 6.4 | 30.9 | 62.7
| MEX | 1.7 | 20.7 | 77.6
| MKK | 3.8 | 25.0 | 71.2
| TSI | 4.9 | 33.3 | 61.8
| 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=G
  |Pval=2E-9
  |OR=1.73
  |ORtxt=[NR]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}