{{Rsnum
|rsid=120074180
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCNQ1
|position=2572882
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|id=607542
|rsnum=120074180
|variant=0006
}}{{ClinVar
|rsid=120074180
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=2594112
|CHROM=11
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=KCNQ1:3784
|GENE_NAME=KCNQ1
|GENE_ID=3784
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.2594112C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607542.0006
|CLNSIG=5
|CLNCUI=C0035828
|CLNDBN=Long QT syndrome 1; Long QT syndrome, LQT1 subtype; not provided
|Disease=Long QT syndrome 1; Long QT syndrome; not provided
|CLNACC=RCV000003266.1; RCV000046135.2; RCV000057769.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1129:NBK1405:C0035828:192500:101016:20852007; CN177655
}}{{PMID Auto
|PMID=1584047
|Title=Simultaneous analysis for testing of models and parameter estimation.
}}

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

{{PMID Auto
|PMID=9323054
|Title=Dominant-negative KvLQT1 mutations underlie the LQT1 form of 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=11216980
|Title=A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics.
}}

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