Gene: KCNH2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2 		0.420 Biomarker disease GENOMICS_ENGLAND Computational Analysis of the Mode of Action of Disopyramide and Quinidine on hERG-Linked Short QT Syndrome in Human Ventricles. 29085299 2017
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2 		0.420 GeneticVariation disease BEFREE In the subgroup of carriers with syncope and/or cardiac arrest (n=10, 90% women), K897T-KCNH2 polymorphism (p=0.02), periodic paralysis (p=0.004), muscle weakness (p=0.04), palpitations (p=0.04), arrhythmias (biventricular VT, p=0.003; polymorphic VT, p=0.009) were observed more frequently. 28336205 2017
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2 		0.420 GeneticVariation disease BEFREE The QTc duration and the frequency of cardiac events (syncope and LQTS-related cardiac arrest/death) were similar among carriers with the five HERG mutations. 11844290 2002
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2 		0.420 Biomarker disease HPO