{{Rsnum
|rsid=111033565
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PRSS1
|position=142751938
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRSS1
}}{{omim
|id=276000
|rsnum=111033565
|variant=0001
}}{{ClinVar
|rsid=111033565
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=142459789
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000402110100
|GENEINFO=PRSS1:5644
|GENE_NAME=PRSS1
|GENE_ID=5644
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.142459789G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK84399; 276000.0001
|CLNSIG=5
|CLNCUI=C0238339; C0238339
|CLNDBN=Hereditary pancreatitis
|Disease=Hereditary pancreatitis
|CLNACC=RCV000012651.23
|Tags=PM;PMC;S3D;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK84399:C0238339:167800:676:68072000
|CLNORIGIN=1
}}{{PMID|1720414}} Monoclonal antibodies which identify carbohydrate-defined MHC class I epitopes.

{{PMID|8841182}} Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.

{{PMID|9557894}} Heterogeneity in hereditary pancreatitis.

{{PMID|16885867}} Estimation of the prevalence and incidence of chronic pancreatitis and its complications.

{{PMID|18286680|OA=1
}} Role of genetic disorders in acute recurrent pancreatitis.

{{PMID|20001681}} Prevalence of pancreatic diabetes in patients carrying mutations or polymorphisms of the PRSS1 gene in the Han population.