[PMID 19019189] Common candidate gene variants are associated with QT interval duration in the general population.

[PMID 19214780] 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] 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.

rs2234916

Parent Gene: KCNE2

Importance: 1
Less common allele: G = 0%
More common allele: A = 100%
My Genotype: Log In