{{Rsnum
|rsid=121909293
|Gene=CTRC
|Chromosome=1
|position=15445717
|Orientation=plus
|GMAF=0.004132
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CTRC
}}{{omim
|id=601405
|rsnum=121909293
|variant=0001
}}{{ClinVar
|rsid=121909293
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=15445717
|CHROM=1
|GMAF=0.0041
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05040016110100
|GENEINFO=CTRC:11330
|GENE_NAME=CTRC
|GENE_ID=11330
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.15445717C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_007272.2:c.760C>T; 601405.0001
|CLNSIG=255
|CLNCUI=C1969419
|CLNDBN=Pancreatitis, chronic, susceptibility to; Hereditary pancreatitis
|Disease=Pancreatitis; Hereditary pancreatitis
|CLNACC=RCV000008657.1; RCV000119045.1
|Tags=PM;S3D;NSM;REF;ASP;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9959; 0.004132
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1969419; NBK84399:C0238339:167800:ORPHA676:68072000
|COMMON=1
}}