{{Rsnum
|rsid=199472730
|Chromosome=11
|position=2572895
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=KCNQ1
|Gene_s=KCNQ1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=G,T
|CHROM=11
|CLNACC=RCV000046141.2; RCV000057774.1; RCV000046142.2; RCV000057775.1
|CLNALLE=1; 2
|CLNDBN=Long QT syndrome, LQT1 subtype; not provided
|CLNDSDB=MedGen
|CLNDSDBID=CN177655
|CLNHGVS=NC_000011.9:g.2594125C>G; NC_000011.9:g.2594125C>T
|CLNORIGIN=1
|CLNSIG=1
|Disease=Long QT syndrome; not provided
|FwdALT=G,T
|FwdREF=C
|GENEINFO=KCNQ1:3784
|GENE_ID=3784
|GENE_NAME=KCNQ1
|REF=C
|RSPOS=2594125
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050368000000000002100100
|WGT=0
|dbSNPBuildID=136
|rsid=199472730
}}{{PMID Auto
|PMID=16414944
|Title=Genetic testing in the long QT syndrome: development and validation of an efficient approach to genotyping in clinical practice.
}}

{{PMID Auto
|PMID=21241
|Title=A sex difference in the interaction between promethazine and morphine in the mouse.
}}

{{PMID Auto
|PMID=12442276
|Title=KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
|OA=1
}}

{{PMID Auto
|PMID=15192825
|Title=[The mutation scanning of KCNQ1 gene for 31 long QT syndrome families].
}}

{{PMID Auto
|PMID=15840476
|Title=Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.
}}

{{PMID Auto
|PMID=16831322
|Title=[Novel mutations of potassium channel KCNQ1 S145L and KCNH2 Y475C genes in Chinese pedigrees of long QT syndrome].
}}

{{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
}}