{{Rsnum
|rsid=80358272
|Chromosome=1
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=KCNQ4
|position=40784304
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ4
}}{{omim
|id=603537
|rsnum=80358272
|variant=0008
}}{{ClinVar
|rsid=80358272
|Reversed=0
|FwdREF=C
|FwdALT=
|REF=GC
|ALT=G
|RSPOS=40784302
|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.40784304delC
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_004700.3:c.211delC; NBK1209; 603537.0008
|CLNSIG=5
|CLNCUI=C2677637; C2677637
|CLNDBN=DFNA 2 Nonsyndromic Hearing Loss
|Disease=DFNA 2 Nonsyndromic Hearing Loss
|CLNACC=RCV000006626.1
|Tags=PM;PMC;SLO;NSF;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1209:C2677637:600101:ORPHA90635
}}{{PMID Auto
|PMID=16596322
|Title=A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype-phenotype correlation.
}}