{{Rsnum
|rsid = 28937890
|Gene = WFS1
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=4
|position=6301966
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WFS1
}}{{omim
|desc=WOLFRAM SYNDROME
|id=606201
|rsnum=28937890
|variant=0003
}}
{{ neighbor
| rsid = 28937893
| distance = 25
}}
{{ neighbor
| rsid = 28937895
| distance = 321
}}

{{ClinVar
|rsid=28937890
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=6303693
|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.6303693C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606201.0003
|CLNSIG=5
|CLNCUI=C0043207
|CLNDBN=Diabetes mellitus AND insipidus with optic atrophy AND deafness
|Disease=Diabetes mellitus AND insipidus with optic atrophy AND deafness
|CLNACC=RCV000004767.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK4144:C0043207:222300:3463:70694009
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}