{{Rsnum
|rsid=104894252
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNQ1
|position=2570715
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNQ1
}}{{omim
|id=607542
|rsnum=104894252
|variant=0003
}}{{ClinVar
|rsid=104894252
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=2591945
|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.2591945G>A; NC_000011.9:g.2591945G>C
|CLNORIGIN=1
|CLNSRCID=
607542.0003
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000003261.1; RCV000046083.2; RCV000057702.1; RCV000057703.1
|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|8528244}} Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.

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

{{PMID|10376919}} Functional effects of mutations in KvLQT1 that cause long QT syndrome.

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