{{Rsnum
|rsid=121918152
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PROC
|position=127426207
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PROC
}}{{omim
|id=612283
|rsnum=121918152
|variant=0013
}}
{{omim
|id=176860
|rsnum=121918152
}}{{ClinVar
|rsid=121918152
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=128183783
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PROC:5624
|GENE_NAME=PROC
|GENE_ID=5624
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.128183783C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612283.0013
|CLNSIG=5
|CLNCUI=C2674321
|CLNDBN=Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant
|Disease=Thrombophilia
|CLNACC=RCV000000703.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2674321:176860:745
}}