{{Rsnum
|rsid=120074181
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNQ1
|position=2572981
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|id=607542
|rsnum=120074181
|variant=0007
}}{{ClinVar
|rsid=120074181
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=2594211
|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; 2
|CLNHGVS=NC_000011.9:g.2594211G>A; NC_000011.9:g.2594211G>C
|CLNORIGIN=1
|CLNSRCID=
607542.0007
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000003262.1; RCV000046152.2; RCV000057797.1; RCV000057798.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|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=10376919
|Title=Functional effects of mutations in KvLQT1 that cause long QT syndrome.
}}

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

{{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.
}}