{{Rsnum
|rsid=151344631
|Chromosome=11
|position=2571333
|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
|CHROM=11
|CLNACC=RCV000030815.1; RCV000046099.2; RCV000057723.2
|CLNALLE=1
|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
|CLNHGVS=NC_000011.9:g.2592563G>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607542.0040
|Disease=Long QT syndrome 1; Long QT syndrome; not provided
|FwdALT=A
|FwdREF=G
|GENEINFO=KCNQ1:3784
|GENE_ID=3784
|GENE_NAME=KCNQ1
|REF=G
|RSPOS=2592563
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=133
|rsid=151344631
}}{{PMID Auto
|PMID=18580685
|Title=A KCNQ1 V205M missense mutation causes a high rate of long QT syndrome in a First Nations community of northern British Columbia: a community-based approach to understanding the impact.
}}

{{PMID Auto
|PMID=20421371
|Title=Mechanistic basis for LQT1 caused by S3 mutations in the KCNQ1 subunit of IKs.
|OA=1
}}