{{Rsnum
|rsid=34150427
|Gene=KCNQ1
|Chromosome=11
|position=2847914
|Orientation=plus
|GMAF=0.004591
|Gene_s=KCNQ1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|rsid=34150427
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=2869144
|CHROM=11
|GMAF=0.005
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000040116100100
|GENEINFO=KCNQ1:3784
|GENE_NAME=KCNQ1
|GENE_ID=3784
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.2869144G>A
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Cardiac arrhythmia; not provided
|Disease=Cardiac arrhythmia; not provided
|Tags=PM;PMC;SLO;VLD;GNO;KGPhase1;KGPROD;OTHERKG;LSD
|CAF=0.9954; 0.004591
|CLNACC=RCV000030110.1; RCV000057651.1
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C0003811:115000
|COMMON=1
}}

{{PMID Auto
|PMID=14661677
|Title=Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome.
}}

{{PMID Auto
|PMID=15913580
|Title=Sudden infant death syndrome: how significant are the cardiac channelopathies?
}}

{{PMID Auto
|PMID=19841300
|Title=Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}