{{Rsnum
|rsid=121909294
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CTRC
|position=15440524
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CTRC
}}{{omim
|id=601405
|rsnum=121909294
|variant=0003
}}{{ClinVar
|rsid=121909294
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=15440524
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000605000002110100
|GENEINFO=CTRC:11330
|GENE_NAME=CTRC
|GENE_ID=11330
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.15440524G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_007272.2:c.164G>A; 601405.0003
|CLNSIG=255
|CLNCUI=C1969419
|CLNDBN=Pancreatitis, chronic, susceptibility to; Hereditary pancreatitis
|Disease=Pancreatitis; Hereditary pancreatitis
|CLNACC=RCV000008659.1; RCV000119047.1
|Tags=PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1969419; NBK84399:C0238339:167800:ORPHA676:68072000
}}