{{Rsnum
|rsid=2771051
|Chromosome=9
|position=117525430
|Orientation=plus
|GMAF=0.4945
|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 | 13.3 | 49.6 | 37.2
| HCB | 59.9 | 33.6 | 6.6
| JPT | 54.9 | 38.1 | 7.1
| YRI | 16.3 | 48.3 | 35.4
| ASW | 19.3 | 45.6 | 35.1
| CHB | 59.9 | 33.6 | 6.6
| CHD | 60.6 | 34.9 | 4.6
| GIH | 28.7 | 44.6 | 26.7
| LWK | 11.8 | 48.2 | 40.0
| MEX | 34.5 | 60.3 | 5.2
| MKK | 15.4 | 42.9 | 41.7
| TSI | 9.8 | 58.8 | 31.4
| 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=4E-9
  |OR=1.49
  |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 | Illumina Human 1M}}