{{Rsnum
|rsid=1910358
|Chromosome=5
|position=23907464
|Orientation=plus
|GMAF=0.3095
|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 | 9.7 | 42.5 | 47.8
| HCB | 18.7 | 43.3 | 38.1
| JPT | 17.0 | 54.5 | 28.6
| YRI | 5.4 | 33.3 | 61.2
| ASW | 5.4 | 48.2 | 46.4
| CHB | 18.7 | 43.3 | 38.1
| CHD | 19.6 | 47.7 | 32.7
| GIH | 8.9 | 41.6 | 49.5
| LWK | 1.8 | 25.5 | 72.7
| MEX | 19.0 | 55.2 | 25.9
| MKK | 3.8 | 37.8 | 58.3
| TSI | 3.9 | 37.3 | 58.8
| 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=G
  |Pval=7E-9
  |OR=2.03
  |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}}