{{Rsnum
|rsid=6764623
|Chromosome=3
|position=1004354
|Orientation=plus
|GMAF=0.3329
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 56.4 | 38.2 | 5.5
| HCB | 20.0 | 57.8 | 22.2
| JPT | 26.7 | 51.1 | 22.2
| YRI | 44.4 | 43.7 | 12.0
| ASW | 41.1 | 42.9 | 16.1
| CHB | 20.0 | 57.8 | 22.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 37.1 | 49.5 | 13.4
| LWK | 35.2 | 55.6 | 9.3
| MEX | 63.6 | 32.7 | 3.6
| MKK | 42.8 | 44.1 | 13.2
| TSI | 56.4 | 38.6 | 5.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23650146
  |Trait=Venous thromboembolism
  |Title=A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
  |RiskAllele=C
  |Pval=2E-6
  |OR=1.18
  |ORtxt=[1.10-1.26]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}