{{Rsnum
|rsid=9804128
|Chromosome=1
|position=18098517
|Orientation=plus
|GMAF=0.3017
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 61.1 | 37.2 | 1.8
| HCB | 69.3 | 29.2 | 1.5
| JPT | 76.8 | 22.3 | 0.9
| YRI | 18.4 | 43.5 | 38.1
| ASW | 22.8 | 54.4 | 22.8
| CHB | 69.3 | 29.2 | 1.5
| CHD | 61.5 | 35.8 | 2.8
| GIH | 54.0 | 36.0 | 10.0
| LWK | 26.4 | 45.5 | 28.2
| MEX | 66.7 | 31.6 | 1.8
| MKK | 22.7 | 51.9 | 25.3
| TSI | 57.8 | 30.4 | 11.8
| 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=A
  |Pval=2E-9
  |OR=1.71
  |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}}