{{Rsnum
|rsid=74315205
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=4
|Orientation=plus
|Gene=WFS1
|position=6302385
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WFS1
}}{{omim
|id=606201
|desc=WFS1 GENE; WFS1
|rsnum=74315205
}}
{{omim
|id=606201
|rsnum=74315205
|variant=0020
}}{{ClinVar
|rsid=74315205
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=6304112
|CHROM=4
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=WFS1:7466
|GENE_NAME=WFS1
|GENE_ID=7466
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.6304112G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK4144; 606201.0020
|CLNSIG=5
|CLNCUI=C1857286; C1833021
|CLNDBN=Wolfram-like syndrome, autosomal dominant; WFS1-Related Disorders
|Disease=Wolfram-like syndrome; WFS1-Related Disorders
|CLNACC=RCV000004784.1; RCV000020637.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C1857286:614296:3463; NBK1434:NBK4144:C1833021:600965:90635
}}{{PMID Auto
|PMID=16648378
|Title=Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene.
|OA=1
}}