{{Rsnum
|rsid=2234916
|Gene=KCNE2
|Chromosome=21
|position=34370500
|Orientation=plus
|GMAF=0.001837
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=KCNE2
}}{{PharmGKB
|RSID=rs2234916
|Name_s=KCNE2:T8A
|Gene_s=FAM165B, KCNE2
|Feature=NA, Exon/NonSyn
|Evidence=PubMed ID:14665560; PubMed ID:17534376
|Annotation=There is conflicting evidence as to whether this SNP predisposes people to drug-induced arrhythmia.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Curated
|PharmGKB Accession ID=PA161145087
}}

{{ClinVar
|rsid=2234916
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=35742799
|CHROM=21
|GMAF=0.0018
|dbSNPBuildID=98
|SSR=0
|SAO=1
|VP=0x050178000000040516100100
|GENEINFO=KCNE2:9992
|GENE_NAME=KCNE2
|GENE_ID=9992
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000021.8:g.35742799A>G
|CLNORIGIN=1
|CLNSIG=1
|Tags=PM;TPA;PMC;SLO;VLD;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD
|CAF=0.9982; 0.001837
|COMMON=1
|CLNACC=RCV000058368.1
|CLNDBN=not provided
|Disease=not provided
}}

{{PMID|19019189|OA=1
}} Common candidate gene variants are associated with QT interval duration in the general population.

{{PMID|19214780|OA=1
}} In silico investigations on functional and haplotype tag SNPs associated with congenital long QT syndromes (LQTSs).

{{PMID|15599}} Pyrrolo(1,4)benzodiazepine antitumor antibiotics. In vitro interaction of anthramycin, sibiromycin and tomaymycin with DNA using specifically radiolabelled molecules.

{{PMID|10984545|OA=1
}} A common polymorphism associated with antibiotic-induced cardiac arrhythmia.

{{PMID|11468227}} Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.

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

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

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

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}