Disease: Atrial Fibrillation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.340 GeneticVariation disease BEFREE In our research, we found that KCNE2 rs8134775 was associated with a decreased AF risk in the allele model (OR = 0.70; 95% CI: 0.50-0.97; p = 0.034). 31270966 2019
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.340 Biomarker disease BEFREE We aimed to investigate if mutations in potassium-channel β-subunits KCNE2 and KCNE3 are associated with early-onset lone AF. 24796621 2014
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.340 GeneticVariation disease LHGDN Thus, KCNE2 R27C is a gain-of-function mutation associated with the initiation and/or maintenance of AF. 15368194 2004
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.340 Biomarker disease CTD_human Thus, KCNE2 R27C is a gain-of-function mutation associated with the initiation and/or maintenance of AF. 15368194 2004
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.340 GeneticVariation disease BEFREE Thus, KCNE2 R27C is a gain-of-function mutation associated with the initiation and/or maintenance of AF. 15368194 2004
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.340 GeneticVariation disease BEFREE On the other hand, researchers in Taiwan reported that a nonsynonymous single nucleotide polymorphism of the LQT5 gene (I(Ks) beta-subunit) is associated with atrial fibrillation. 14631130 2003