{{Rsnum
|rsid=80358275
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=KCNQ4
|position=40819423
|Gene_s=KCNQ4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=80358275
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=40819423
|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.40819423A>T
|CLNORIGIN=0
|CLNSIG=5
|CLNCUI=600101
|CLNDBN=DFNA 2 Nonsyndromic Hearing Loss
|Tags=PM;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000020612.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1209:C2677637:600101:ORPHA90635
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_004700.3:c.785A>T; NBK1209
|Disease=DFNA 2 Nonsyndromic Hearing Loss
}}