{{Rsnum
|rsid=120074194
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNQ1
|position=2572871
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|id=607542
|rsnum=120074194
|variant=0034
}}{{ClinVar
|rsid=120074194
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=2594101
|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.2594101G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607542.0034
|CLNSIG=5
|CLNCUI=C0035828
|CLNDBN=Long QT syndrome 1; KCNQ1-related Jervell and Lange-Nielsen syndrome; Long QT syndrome, LQT1 subtype; not provided
|Disease=Long QT syndrome 1; KCNQ1-related Jervell and Lange-Nielsen syndrome; Long QT syndrome; not provided
|CLNACC=RCV000003295.1; RCV000046132.2; RCV000046133.2; RCV000057766.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen
|CLNDSDBID=NBK1129:NBK1405:C0035828:192500:101016:20852007; CN177652; CN177655
}}{{PMID|158404}} Vasoactive intestinal polypeptide (VIP): distribution in normal human brain and in Huntington's disease.

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

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

{{PMID|12051962}} Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome.

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

{{PMID|15466642}} Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes.