{{Rsnum
|rsid=6858430
|Chromosome=4
|position=174894978
|Orientation=plus
|GMAF=0.3338
|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 | 63.7 | 32.7 | 3.5
| HCB | 31.1 | 49.6 | 19.3
| JPT | 19.6 | 50.9 | 29.5
| YRI | 50.0 | 43.2 | 6.8
| ASW | 47.4 | 49.1 | 3.5
| CHB | 31.1 | 49.6 | 19.3
| CHD | 32.4 | 41.7 | 25.9
| GIH | 60.4 | 35.6 | 4.0
| LWK | 50.0 | 44.4 | 5.6
| MEX | 25.9 | 50.0 | 24.1
| MKK | 65.8 | 32.3 | 1.9
| TSI | 57.8 | 38.2 | 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=G
  |Pval=1E-8
  |OR=1.62
  |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}}