{{Rsnum
|rsid=80358279
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNQ4
|position=40819926
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ4
}}{{omim
|id=603537
|rsnum=80358279
|variant=0009
}}{{ClinVar
|rsid=80358279
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=40819926
|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
|CLNHGVS=NC_000001.11:g.40819926G>A
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_004700.3:c.886G>A; NBK1209; 603537.0009
|CLNSIG=5
|CLNCUI=C2677637; C2677637
|CLNDBN=DFNA 2 Nonsyndromic Hearing Loss
|Disease=DFNA 2 Nonsyndromic Hearing Loss
|CLNACC=RCV000006627.1
|Tags=PM;PMC;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1209:C2677637:600101:ORPHA90635
}}{{PMID|18030493}} A novel KCNQ4 pore-region mutation (p.G296S) causes deafness by impairing cell-surface channel expression.