{{Rsnum
|rsid=80358274
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNQ4
|position=40819416
|Gene_s=KCNQ4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80358274
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=40819416
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000a05000002110100
|GENEINFO=KCNQ4:9132
|GENE_NAME=KCNQ4
|GENE_ID=9132
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.40819416G>A
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=600101
|CLNDBN=DFNA 2 Nonsyndromic Hearing Loss
|Tags=PM;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000020611.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1209:C2677637:600101:ORPHA90635
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_004700.3:c.778G>A; NBK1209
|Disease=DFNA 2 Nonsyndromic Hearing Loss
}}