{{Rsnum
|rsid=111033566
|Chromosome=7
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=PRSS1
|position=142750600
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PRSS1
}}{{omim
|id=276000
|rsnum=111033566
|variant=0002
}}{{ClinVar
|rsid=111033566
|Reversed=0
|FwdREF=A
|FwdALT=C,T
|REF=A
|ALT=C,T
|RSPOS=142458451
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=PRSS1:5644
|GENE_NAME=PRSS1
|GENE_ID=5644
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000007.13:g.142458451A>C; NC_000007.13:g.142458451A>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK84399; 276000.0002; 276000.0004
|CLNSIG=5
|CLNCUI=C0238339; C0238339
|CLNDBN=Hereditary pancreatitis
|Disease=Hereditary pancreatitis
|CLNACC=RCV000031923.1; RCV000012652.17
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK84399:C0238339:167800:676:68072000
}}{{PMID Auto
|PMID=185115
|Title=[Participation of the beta-receptor system in the genesis of the carotid aortic baroreceptor reflex in the dog (author's transl)].
}}

{{PMID Auto
|PMID=9633818
|Title=Mutations of the cationic trypsinogen in hereditary pancreatitis.
}}

{{PMID Auto
|PMID=11719509
|Title=Hereditary pancreatitis caused by a novel PRSS1 mutation (Arg-122 --> Cys) that alters autoactivation and autodegradation of cationic trypsinogen.
}}

{{PMID Auto
|PMID=11788572
|Title=Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis.
|OA=1
}}

{{PMID Auto
|PMID=11842279
|Title=R116C mutation of cationic trypsinogen in a Turkish family with recurrent pancreatitis illustrates genetic microheterogeneity of hereditary pancreatitis.
}}

{{PMID Auto
|PMID=12011155
|Title=Mutations in the pancreatic secretory trypsin inhibitor gene (PSTI/SPINK1) rather than the cationic trypsinogen gene (PRSS1) are significantly associated with tropical calcific pancreatitis.
|OA=1
}}