{{Rsnum
|rsid=28937588
|Gene=KCNQ4
|Chromosome=1
|position=40819893
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ4
}}[[deafness]]
{{omim
|desc=DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 2
|id=603537
|rsnum=28937588
|variant=0001
}}
{{ neighbor
| rsid = 28937589
| distance = 431
}}
{{omim
|id=603537
|rsnum=28937588
|variant=0004
}}{{ClinVar
|rsid=28937588
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=40819893
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000a05000002110100
|GENEINFO=KCNQ4:9132
|GENE_NAME=KCNQ4
|GENE_ID=9132
|WGT=1
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000001.11:g.40819893G>A; NC_000001.11:g.40819893G>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_004700.3:c.853G>A; NBK1209; 603537.0001; NM_004700.3:c.853G>T; 603537.0004
|CLNSIG=5
|CLNCUI=C2677637; C2677637,C2677637; C2677637
|CLNDBN=DFNA 2 Nonsyndromic Hearing Loss
|Disease=DFNA 2 Nonsyndromic Hearing Loss
|CLNACC=RCV000006619.1; RCV000006622.1
|Tags=PM;PMC;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1209:C2677637:600101:ORPHA90635
}}{{PMID Auto
|PMID=10025409
|Title=KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness.
}}

{{PMID Auto
|PMID=10369879
|Title=Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.
}}