{{Rsnum
|rsid=120074182
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=KCNQ1
|position=2583448
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|id=607542
|rsnum=120074182
|variant=0008
}}{{ClinVar
|rsid=120074182
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=2604678
|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.2604678C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607542.0008
|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=RCV000003263.1; RCV000046165.2; RCV000057808.1
|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=1546664
|Title=Intraaortic debris as a potential source of embolic stroke.
}}

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

{{PMID Auto
|PMID=15051636
|Title=Compound mutations: a common cause of severe long-QT syndrome.
}}