{{Rsnum
|rsid=80358271
|Chromosome=1
|Orientation=plus
|geno1=(-;-)
|geno2=(-;CAGCGCTCCTCGG)
|geno3=(CAGCGCTCCTCGG;CAGCGCTCCTCGG)
|Gene=KCNQ4
|position=40784304
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ4
}}{{omim
|id=603537
|rsnum=80358271
|variant=0005
}}{{ClinVar
|rsid=80358271
|Reversed=0
|FwdREF=CAGCGCTCCTCGG
|FwdALT=
|REF=CCAGCGCTCCTCGG
|ALT=C
|RSPOS=40784303
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168001205000002110200
|GENEINFO=KCNQ4:9132
|GENE_NAME=KCNQ4
|GENE_ID=9132
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.40784304_40784316delCAGCGCTCCTCGG
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_004700.3:c.211_223delCAGCGCTCCTCGG; NBK1209; 603537.0005
|CLNSIG=5
|CLNCUI=C2677637; C2677637
|CLNDBN=DFNA 2 Nonsyndromic Hearing Loss
|Disease=DFNA 2 Nonsyndromic Hearing Loss
|CLNACC=RCV000006623.1
|Tags=PM;PMC;SLO;NSF;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1209:C2677637:600101:ORPHA90635
}}{{PMID|10369879}} Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.