{{Rsnum
|rsid=2321744
|Chromosome=13
|position=34032049
|Orientation=minus
|GMAF=0.1359
|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 | 14.2 | 84.1
| HCB | 0.7 | 21.3 | 77.9
| JPT | 0.9 | 24.1 | 75.0
| YRI | 8.8 | 29.3 | 61.9
| ASW | 5.3 | 33.3 | 61.4
| CHB | 0.7 | 21.3 | 77.9
| CHD | 2.8 | 14.8 | 82.4
| GIH | 5.0 | 39.0 | 56.0
| LWK | 7.4 | 29.6 | 63.0
| MEX | 3.5 | 38.6 | 57.9
| MKK | 18.2 | 49.4 | 32.5
| TSI | 0.0 | 12.7 | 87.3
| 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=
  |Pval=1E-9
  |OR=2.04
  |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}}