{{Rsnum
|rsid=387906930
|Chromosome=4
|position=6301846
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=WFS1
|Gene_s=WFS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=4
|CLNACC=RCV000023514.1; RCV000023515.1
|CLNALLE=1
|CLNDBN=Wolfram-like syndrome, autosomal dominant; Diabetes mellitus AND insipidus with optic atrophy AND deafness
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1857286:614296:3463; NBK4144:C0043207:222300:3463:70694009
|CLNHGVS=NC_000004.11:g.6303573C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606201.0028
|Disease=Wolfram-like syndrome; Diabetes mellitus AND insipidus with optic atrophy AND deafness
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=6303573
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906930
|GENEINFO=WFS1:7466
|GENE_ID=7466
|GENE_NAME=WFS1
}}