The rs2236609 Polymorphism Is Related to Increased Risk Susceptibility of Atrial Fibrillation.

doi:10.1159/000506997

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

The rs2236609 Polymorphism Is Related to Increased Risk Susceptibility of Atrial Fibrillation.

Public health genomics - 1 Jan 2020

Alzoughool Foad, Atoum Manar, Abu-Awad Aymen, Ghanma Issa, Halalsheh Raed

Abstract excerpt

INTRODUCTION: Genetic variations in the slow component of the delayed rectifier potassium channels (IKs) are reported to contribute to an increased susceptibility to arrhythmias. This study aims to investigate the frequency and the possible association of the rs2236609 polymorphism in the KCNE1 gene and the risk of atrial fibrillation (AF). METHODS: This was a case-control study that recruited 100 patients...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Atrial Fibrillation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Case-Control Studies

Share to Genetic Predisposition to Disease

Share to Genetic Testing

Share to Jordan

Share to Polymorphism, Single Nucleotide

Share to Potassium Channels, Voltage-Gated

Share to Protective Factors

Source

Open in PubMed

Identifiers

PMID: 32316011
DOI: 10.1159/000506997

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The rs2236609 Polymorphism Is Related to Increased Risk Susceptibility of Atrial Fibrillation.PMID 32316011Read ↗

KCNE1 rs1805127 polymorphism increases the risk of atrial fibrillation: a meta-analysis of 10 studies.Semantic proximity Read ↗

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

Association of KCNE1 genetic polymorphisms with atrial fibrillation in a Chinese Han population.Semantic proximity Read ↗

The single nucleotide polymorphisms of I(Ks) potassium channel genes and their association with atrial fibrillation in a Chinese population.Semantic proximity Read ↗

CASP3 genetic variants and susceptibility to atrial fibrillation in Chinese Han population.Semantic proximity Read ↗

The role of common genetic variants in atrial fibrillation.Semantic proximity Read ↗

Molecular genetics of atrial fibrillation.Semantic proximity Read ↗

Heritability of Atrial Fibrillation.Semantic proximity Read ↗

Association Between Rs3807989 Polymorphism in Caveolin-1 (CAV1) Gene and Atrial Fibrillation: A Meta-Analysis.Semantic proximity Read ↗

The genetics of atrial fibrillation.Semantic proximity Read ↗

Association between KCNE1 G38S gene polymorphism and risk of atrial fibrillation: A PRISMA-compliant meta-analysis.Semantic proximity Read ↗

[Genetics of atrial fibrillation: rare mutations, common variants and clinical relevance?].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.