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 		0.020 Biomarker disease BEFREE This study focuses on investigating the potential variants on SCN5A, KCNQ1, and KCNH2 contributing to AMI with VA in a Chinese population. 31751991 2020
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2 		0.020 GeneticVariation disease BEFREE Thus, patients with an acute MI carrying the KCNH2-K897T polymorphism had an 8-fold greater risk of experiencing TdP compared with controls (95% confidence interval = 2-40). 22338672 2012