SNP information rs1805127

Research and publications:

  17210   [Carbogen therapy of acute cochlear disorders].

  7828904   Polymorphism of the gene encoding a human minimal potassium ion channel (minK).

  9445165   Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of Long-QT syndrome.

  12402336   DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.

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

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

  15599693   Single nucleotide polymorphism map of five long-QT genes.

  16487223   Genetic polymorphisms in KCNQ1, HERG, KCNE1 and KCNE2 genes in the Chinese, Malay and Indian populations of Singapore.

  17161064   Association of torsades de pointes with novel and known single nucleotide polymorphisms in long QT syndrome genes.

  17210839   Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.

  17227789   The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study.

  17534376   Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects.

  17597962   Mutation screening in KCNQ1, HERG, KCNE1, KCNE2 and SCN5A genes in a long QT syndrome family.

  18426444   Single nucleotide polymorphisms and haplotype of four genes encoding cardiac ion channels in Chinese and their association with arrhythmia.

  18520591   Host cell factor C1 sequence variants are associated with Meniere's disease.

  18674739   Effect of common KCNE1 and SCN5A ion channel gene variants on T-wave alternans, a marker of cardiac repolarization, during clinical exercise stress test: the Finnish Cardiovascular Study.

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

  19305409   Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

  19660109   Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes.

  20400777   Common variants in cardiac ion channel genes are associated with sudden cardiac death.

  20850564   R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation.

  21056700   Lack of replication in polymorphisms reported to be associated with atrial fibrillation.

  21811988   [Association of rs1805127 polymorphism of KCNE1 gene with atrial fibrillation in Uigur population of Xinjiang].

  21967835   The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.

  22581653   Paralogous annotation of disease-causing variants in long QT syndrome genes.

  22934933   A replication study of proposed candidate genes for Meniere's disease and a review of the current status of genetic research.

  23020083   Association of KCNE1 genetic polymorphisms with atrial fibrillation in a Chinese Han population.

  23272793   KCNE genetics and pharmacogenomics in cardiac arrhythmias: much ado about nothing?

  23861362   Interpreting secondary cardiac disease variants in an exome cohort.

  24033266   A systematic approach to assessing the clinical significance of genetic variants.

  24705329   Single-nucleotide variations in cardiac arrhythmias: prospects for genomics and proteomics based biomarker discovery and diagnostics.

  24710009   An Examination of KCNE1 Mutations and Common Variants in Chronic Tinnitus.

  25741868   Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

  26066992   Genetic variants of potassium voltage-gated channel genes (KCNQ1, KCNH2, and KCNE1) affected the risk of atrial fibrillation in elderly patients.

  27509294   Meniere's disease: molecular analysis of aquaporins 2, 3 and potassium channel genes KCNE1 in Brazilian patients.

  28073131   Evaluation of Glutathione Peroxidase and KCNJ11 Gene Polymorphisms in Patients with New Onset Diabetes Mellitus After Renal Transplantation.

  28981946   [Association of KCNE1 and KCNE4 gene polymorphisms with atrial fibrillation among Uygur and Han Chinese populations in Xinjiang].

  29396286   Genetic variants in post myocardial infarction patients presenting with electrical storm of unstable ventricular tachycardia.

  32207011   Variations in the potassium voltage-gated channel subfamily E regulatory subunit 1 gene associated with noise-induced hearing loss in the Chinese population.

  34638656   Towards Understanding the Genetic Nature of Vasovagal Syncope.