{{Rsnum
|rsid=6815916
|Chromosome=4
|position=181631890
|Orientation=plus
|GMAF=0.09091
|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 | 85.7 | 13.4 | 0.9
| HCB | 66.4 | 32.1 | 1.5
| JPT | 72.6 | 25.7 | 1.8
| YRI | 72.6 | 26.7 | 0.7
| ASW | 87.5 | 10.7 | 1.8
| CHB | 66.4 | 32.1 | 1.5
| CHD | 67.9 | 28.4 | 3.7
| GIH | 74.0 | 26.0 | 0.0
| LWK | 83.5 | 15.6 | 0.9
| MEX | 89.5 | 10.5 | 0.0
| MKK | 86.5 | 13.5 | 0.0
| TSI | 90.2 | 9.8 | 0.0
| 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=T
  |Pval=7E-10
  |OR=2.10
  |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}}