{{Rsnum
|rsid=199472815
|Chromosome=11
|position=2778024
|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,C
|CHROM=11
|CLNACC=RCV000046030.2; RCV000046031.2; RCV000057637.1; RCV000046032.2; RCV000057638.1
|CLNALLE=1; 2
|CLNDBN=KCNQ1-related Jervell and Lange-Nielsen syndrome; Long QT syndrome, LQT1 subtype; not provided
|CLNDSDB=MedGen
|CLNDSDBID=CN177652; CN177655
|CLNHGVS=NC_000011.9:g.2799254G>A; NC_000011.9:g.2799254G>C
|CLNORIGIN=1
|CLNSIG=1
|Disease=KCNQ1-related Jervell and Lange-Nielsen syndrome; Long QT syndrome; not provided
|FwdALT=A,C
|FwdREF=G
|GENEINFO=KCNQ1:3784
|GENE_ID=3784
|GENE_NAME=KCNQ1
|REF=G
|RSPOS=2799254
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050168000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199472815
}}{{PMID Auto
|PMID=15840
|Title=The purification and properties of NADP-dependent isocitrate dehydrogenase from ox-heart mitochondria.
}}

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

{{PMID Auto
|PMID=11530100
|Title=A spectrum of functional effects for disease causing mutations in the Jervell and Lange-Nielsen syndrome.
}}

{{PMID Auto
|PMID=12402336
|Title=DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
}}

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

{{PMID Auto
|PMID=15051636
|Title=Compound mutations: a common cause of severe long-QT syndrome.
}}

{{PMID Auto
|PMID=17224687
|Title=Whole blood RNA offers a rapid, comprehensive approach to genetic diagnosis of cardiovascular diseases.
}}

{{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
}}