{{Rsnum
|rsid=121918159
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PROC
|position=127423319
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MIR4783,PROC
}}{{omim
|id=612283
|rsnum=121918159
|variant=0024
}}{{ClinVar
|rsid=121918159
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=128180895
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PROC:5624; MIR4783:100616187
|GENE_NAME=PROC; MIR4783
|GENE_ID=5624; 100616187
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.128180895A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=612283.0024
|CLNSIG=5
|CLNCUI=C2674321
|CLNDBN=Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant
|Disease=Thrombophilia
|CLNACC=RCV000000714.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2674321:176860:745
}}