{{Rsnum
|rsid=2710201
|Chromosome=7
|position=153227808
|Orientation=minus
|GMAF=0.2075
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LOC102723686
|Gene_s=LOC102723686
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.9 | 12.5 | 86.6
| HCB | 0.0 | 14.9 | 85.1
| JPT | 0.0 | 4.4 | 95.6
| YRI | 45.1 | 42.4 | 12.5
| ASW | 33.3 | 38.6 | 28.1
| CHB | 0.0 | 14.9 | 85.1
| CHD | 0.0 | 21.3 | 78.7
| GIH | 1.0 | 12.9 | 86.1
| LWK | 43.0 | 39.3 | 17.8
| MEX | 1.7 | 32.8 | 65.5
| MKK | 23.1 | 46.8 | 30.1
| TSI | 0.0 | 7.9 | 92.1
| 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=3E-9
  |OR=2.50
  |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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}