{{Rsnum
|rsid=28937894
|Gene=WFS1
|Chromosome=4
|position=6301891
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=WFS1
}}[[deafness]]
{{omim
|desc=DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 6
|id=606201
|rsnum=28937894
|variant=0016
}}
{{ neighbor
| rsid = 28937891
| distance = 12
}}
{{ neighbor
| rsid = 28937893
| distance = 50
}}

{{ClinVar
|rsid=28937894
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=6303618
|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.6303618C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606201.0016
|CLNSIG=5
|CLNCUI=C1833021
|CLNDBN=WFS1-Related Disorders
|Disease=WFS1-Related Disorders
|CLNACC=RCV000004780.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:NBK4144:C1833021:600965:90635
}}

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