{{Rsnum
|rsid=2731672
|Chromosome=5
|position=177415473
|Orientation=minus
|GMAF=0.4316
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 7.1 | 23.9 | 69.0
| HCB | 51.8 | 41.6 | 6.6
| JPT | 50.9 | 42.0 | 7.1
| YRI | 32.7 | 46.9 | 20.4
| ASW | 15.8 | 40.4 | 43.9
| CHB | 51.8 | 41.6 | 6.6
| CHD | 65.7 | 31.5 | 2.8
| GIH | 24.8 | 54.5 | 20.8
| LWK | 14.5 | 53.6 | 31.8
| MEX | 19.0 | 46.6 | 34.5
| MKK | 26.9 | 49.4 | 23.7
| TSI | 1.0 | 32.4 | 66.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20303064
|Trait=Activated partial thromboplastin time
|Title=Common Variants of Large Effect in F12, KNG1, and HRG Are Associated with Activated Partial Thromboplastin Time
|RiskAllele=A
|Pval=2E-30
|OR=0.45
|ORtxt=[0.37-0.53] unit decrease
|OA=1
}}

{{omim
|desc=COAGULATION FACTOR XII; F12
|id=610619
|rsnum=2731672
}}

{{omim
|id=188050
|rsnum=2731672
}}

{{PMID Auto GWAS
|PMID=21546496
|Trait=None
|Title=Novel loci involved on platelet function and platelet count identified by a genome-wide study performed in children.
|RiskAllele=
|Pval=0.000001
|OR=None
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=21270443
|Title=KNG1 Ile581Thr and susceptibility to venous thrombosis.
}}

{{PMID Auto GWAS
  |PMID=22916037
  |Trait=Metabolite levels
  |Title=Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.
  |RiskAllele=
  |Pval=3E-14
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{PMID Auto GWAS
  |PMID=23381795
  |Trait=Circulating vasoactive peptide levels
  |Title=Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1.
  |RiskAllele=T
  |Pval=6E-24
  |OR=.02
  |ORtxt=[0.018-0.026] nmol/l increase
  }}

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