{{Rsnum
|rsid=4253399
|Gene=F11
|Chromosome=4
|position=186266940
|Orientation=plus
|GMAF=0.2833
|Gene_s=F11
|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 | 15.9 | 46.9 | 37.2
| HCB | 8.8 | 39.4 | 51.8
| JPT | 12.4 | 37.2 | 50.4
| YRI | 0.7 | 10.9 | 88.4
| ASW | 1.8 | 19.3 | 78.9
| CHB | 8.8 | 39.4 | 51.8
| CHD | 9.2 | 41.3 | 49.5
| GIH | 9.9 | 45.5 | 44.6
| LWK | 0.0 | 12.7 | 87.3
| MEX | 8.6 | 60.3 | 31.0
| MKK | 0.6 | 8.3 | 91.0
| TSI | 15.7 | 47.1 | 37.3
| 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=G
  |Pval=3E-14
  |OR=1.24
  |ORtxt=[1.17-1.31]
  }}

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