{{Rsnum
|rsid=199472751
|Chromosome=11
|position=2583462
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNQ1
|Gene_s=KCNQ1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=A,T
|CHROM=11
|CLNACC=RCV000046177.2; RCV000057822.1; RCV000057823.1
|CLNALLE=1; 2
|CLNDBN=Long QT syndrome, LQT1 subtype; not provided
|CLNDSDB=MedGen
|CLNDSDBID=CN177655
|CLNHGVS=NC_000011.9:g.2604692G>A; NC_000011.9:g.2604692G>T
|CLNORIGIN=1
|CLNSIG=1
|Disease=Long QT syndrome; not provided
|FwdALT=A,T
|FwdREF=G
|GENEINFO=KCNQ1:3784
|GENE_ID=3784
|GENE_NAME=KCNQ1
|REF=G
|RSPOS=2604692
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199472751
}}{{PMID Auto
|PMID=9302275
|Title=Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias.
}}

{{PMID Auto
|PMID=9482580
|Title=Molecular genetics of the long QT syndrome: two novel mutations of the KVLQT1 gene and phenotypic expression of the mutant gene in a large kindred.
}}

{{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=20541041
|Title=Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study.
}}