{{Rsnum
|rsid=193922638
|Chromosome=9
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=CEL
|position=133071278
|Gene_s=CEL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922638
|Reversed=0
|FwdREF=C
|FwdALT=
|REF=GC
|ALT=G
|RSPOS=135946657
|CHROM=9
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.135946665delC
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Maturity-onset diabetes of the young, type 8
|Disease=Maturity-onset diabetes of the young
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000029467.1
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1853297:609812:552
|GENEINFO=CEL:1056
|GENE_ID=1056
|GENE_NAME=CEL
}}{{PMID|16369531}} Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction.