{{Rsnum
|rsid=120074179
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNQ1
|position=2572089
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|id=607542
|rsnum=120074179
|variant=0005
}}{{ClinVar
|rsid=120074179
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=2593319
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=KCNQ1:3784
|GENE_NAME=KCNQ1
|GENE_ID=3784
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000011.9:g.2593319G>A; NC_000011.9:g.2593319G>C; NC_000011.9:g.2593319G>T
|CLNORIGIN=1
|CLNSRCID=
607542.0005; 607542.0035
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000003265.1; RCV000003296.1; RCV000046118.2; RCV000057749.1; RCV000057750.1; RCV000046119.2; RCV000057751.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=Long QT syndrome 1; Long QT syndrome, LQT1 subtype; not provided
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1129:NBK1405:C0035828:192500:101016:20852007; CN177655
|CLNSRC=OMIM Allelic Variant
|Disease=Long QT syndrome 1; Long QT syndrome; not provided
}}{{PMID Auto
|PMID=1475667
|Title=[Periodontitis and caries--"God's punishment"?].
}}

{{PMID Auto
|PMID=8528244
|Title=Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
}}

{{PMID Auto
|PMID=9386136
|Title=KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome.
}}

{{PMID Auto
|PMID=10973849
|Title=Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.
}}

{{PMID Auto
|PMID=12820704
|Title=Mutation analysis in congenital Long QT Syndrome--a case with missense mutations in KCNQ1 and SCN5A.
}}

{{PMID Auto
|PMID=14678125
|Title=Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome.
}}

{{PMID Auto
|PMID=16414944
|Title=Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.
}}