{{Rsnum
|rsid=193922659
|Chromosome=5
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=SPINK1
|position=147831551
|Gene_s=SPINK1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922659
|Reversed=1
|FwdREF=C
|FwdALT=
|REF=TG
|ALT=T
|RSPOS=147211113
|CHROM=5
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.147211114delG
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Hereditary pancreatitis
|Disease=Hereditary pancreatitis
|Tags=RV;PM;PMC;OTHERKG;LSD
|CLNACC=RCV000030460.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK84399:C0238339:167800:676:68072000
|GENEINFO=SPINK1:6690
|GENE_ID=6690
|GENE_NAME=SPINK1
}}{{PMID Auto
|PMID=14722925
|Title=Two novel severe mutations in the pancreatic secretory trypsin inhibitor gene (SPINK1) cause familial and/or hereditary pancreatitis.
}}

{{PMID Auto
|PMID=16823394
|Title=Detection of a large genomic deletion in the pancreatic secretory trypsin inhibitor (SPINK1) gene.
}}

{{PMID Auto
|PMID=16981266
|Title=Association of rare SPINK1 gene mutation with another base substitution in chronic pancreatitis patients.
}}

{{PMID Auto
|PMID=17274009
|Title=Signal peptide variants that impair secretion of pancreatic secretory trypsin inhibitor (SPINK1) cause autosomal dominant hereditary pancreatitis.
|OA=1
}}

{{PMID Auto
|PMID=17568390
|Title=Functional analysis of pancreatitis-associated missense mutations in the pancreatic secretory trypsin inhibitor (SPINK1) gene.
}}