{{Rsnum
|rsid=104893882
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=WFS1
|position=6301696
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WFS1
}}{{omim
|id=606201
|rsnum=104893882
|variant=0018
}}{{ClinVar
|rsid=104893882
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=6303423
|CHROM=4
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=WFS1:7466
|GENE_NAME=WFS1
|GENE_ID=7466
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.6303423A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606201.0018
|CLNSIG=5
|CLNCUI=C1833021
|CLNDBN=WFS1-Related Disorders
|Disease=WFS1-Related Disorders
|CLNACC=RCV000004782.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:NBK4144:C1833021:600965:90635
}}