{{Rsnum
|rsid=80358273
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=KCNQ4
|position=40818518
|Gene_s=KCNQ4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80358273
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=40818518
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000a05000002110100
|GENEINFO=KCNQ4:9132
|GENE_NAME=KCNQ4
|GENE_ID=9132
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.40818518C>G
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=600101
|CLNDBN=DFNA 2 Nonsyndromic Hearing Loss
|Tags=PM;PMC;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000020609.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1209:C2677637:600101:ORPHA90635
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_004700.3:c.546C>G; NBK1209
|Disease=DFNA 2 Nonsyndromic Hearing Loss
}}{{PMID|17033161}} Identification of novel mutations in the KCNQ4 gene of patients with nonsyndromic deafness from Taiwan.