{{Rsnum
|rsid=1799810
|Gene=PROC
|Chromosome=2
|position=127418464
|Orientation=plus
|GMAF=0.3494
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=PROC
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 45.9 | 39.3 | 14.8
| HCB | 62.2 | 35.6 | 2.2
| JPT | 70.5 | 27.3 | 2.3
| YRI | 14.8 | 42.6 | 42.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 62.2 | 35.6 | 2.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20707712
|Trait=None
|Title=A genome-wide association study of self-rated health
|RiskAllele=T
|Pval=0.000009
|OR=0.02
|ORtxt=[NR] unit decrease
|OA=1
}}

{{PMID Auto
|PMID=20031567
|Title=An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: The Women's Genome Health Study.
|OA=1
}}

{{PMID Auto
|PMID=24300144
|Title=[Phenotypic detection and structure analysis of a PC missense mutation (Met406Ile) resulted in venous thromboembolism]
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}