{{Rsnum
|rsid=16991652
|Gene=KCNE2
|Chromosome=21
|position=34370503
|Orientation=plus
|GMAF=0.003673
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=KCNE2
}}{{omim
|id=603796
|rsnum=16991652
|variant=0001
}}{{ClinVar
|rsid=16991652
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=35742802
|CHROM=21
|GMAF=0.0037
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050178000000040516110100
|GENEINFO=KCNE2:9992
|GENE_NAME=KCNE2
|GENE_ID=9992
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000021.8:g.35742802C>G
|CLNORIGIN=0
|CLNSIG=255
|Tags=PM;TPA;PMC;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9963; 0.003673
|CLNACC=RCV000006424.1; RCV000058370.1
|CLNDBN=Long QT syndrome 6, acquired, susceptibility to; not provided
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603796.0001
|COMMON=1
|Disease=Long QT syndrome 6; not provided
}}{{PMID Auto
|PMID=10219239
|Title=MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia.
}}

{{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=14760488
|Title=Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.
}}

{{PMID Auto
|PMID=17210839
|Title=Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.
}}

{{PMID Auto
|PMID=20981092
|Title=A map of human genome variation from population-scale sequencing.
|OA=1
}}