Disease: Cardiac Arrest ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1805123
rs1805123
Entrez Id: 3757
Gene Symbol: KCNH2
KCNH2
CUI: C0018790
Disease:
Cardiac Arrest 		0.010 GeneticVariation 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