{{Rsnum
|rsid=6536024
|Chromosome=4
|position=154622217
|Orientation=plus
|GMAF=0.4922
|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 | 33.6 | 45.1 | 21.2
| HCB | 40.1 | 48.9 | 10.9
| JPT | 40.7 | 53.1 | 6.2
| YRI | 8.2 | 49.7 | 42.2
| ASW | 15.8 | 47.4 | 36.8
| CHB | 40.1 | 48.9 | 10.9
| CHD | 34.9 | 50.5 | 14.7
| GIH | 30.7 | 41.6 | 27.7
| LWK | 13.6 | 48.2 | 38.2
| MEX | 13.8 | 41.4 | 44.8
| MKK | 9.0 | 41.7 | 49.4
| TSI | 25.5 | 45.1 | 29.4
| 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-13
  |OR=1.25
  |ORtxt=[1.18-1.32]
  }}

{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}