{{Rsnum
|rsid=120074184
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNQ1
|position=2583453
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|id=607542
|rsnum=120074184
|variant=0012
}}{{ClinVar
|rsid=120074184
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=2604683
|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.2604683G>A; NC_000011.9:g.2604683G>C; NC_000011.9:g.2604683G>T
|CLNORIGIN=1
|CLNSRCID=
607542.0012
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000003271.1; RCV000046167.2; RCV000057810.1; RCV000046168.2; RCV000057811.1; RCV000046169.2; RCV000057812.1
|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=8872472
|Title=KVLQT1 mutations in three families with familial or sporadic long QT syndrome.
}}

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

{{PMID Auto
|PMID=9693036
|Title=Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.
}}

{{PMID Auto
|PMID=9799083
|Title=Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome.
}}

{{PMID Auto
|PMID=10220144
|Title=Novel KCNQ1 and HERG missense mutations in Dutch long-QT families.
}}

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

{{PMID Auto
|PMID=12702160
|Title=KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.
|OA=1
}}

{{PMID Auto
|PMID=19716085
|Title=Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
|OA=1
}}

{{PMID Auto
|PMID=15840476
|Title=Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
}}