{{Rsnum
|rsid=7648704
|Chromosome=3
|position=32900360
|Orientation=plus
|GMAF=0.354
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 10.7 | 47.3 | 42.0
| HCB | 8.8 | 34.6 | 56.6
| JPT | 5.3 | 45.1 | 49.6
| YRI | 30.8 | 48.6 | 20.5
| ASW | 17.5 | 45.6 | 36.8
| CHB | 8.8 | 34.6 | 56.6
| CHD | 5.5 | 38.5 | 56.0
| GIH | 9.0 | 39.0 | 52.0
| LWK | 40.0 | 42.7 | 17.3
| MEX | 12.1 | 56.9 | 31.0
| MKK | 23.1 | 46.8 | 30.1
| TSI | 9.8 | 51.0 | 39.2
| 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=1E-9
  |OR=1.56
  |ORtxt=[NR]
  |OA=1
}}

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