Disease: Brugada Syndrome 8 ×
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs794727637
rs794727637
Entrez Id: 10021
Gene Symbol: HCN4
HCN4
CUI: C2751083
Disease:
Brugada Syndrome 8 		T 0.700 CausalMutation CLINVAR HCN4 mutation as a molecular explanation on patients with bradycardia and non-compaction cardiomyopathy. 26206080 2015
dbSNP: rs794727637
rs794727637
Entrez Id: 10021
Gene Symbol: HCN4
HCN4
CUI: C2751083
Disease:
Brugada Syndrome 8 		T 0.700 CausalMutation CLINVAR HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy. 25145517 2014
dbSNP: rs794727637
rs794727637
Entrez Id: 10021
Gene Symbol: HCN4
HCN4
CUI: C2751083
Disease:
Brugada Syndrome 8 		T 0.700 CausalMutation CLINVAR The symptom complex of familial sinus node dysfunction and myocardial noncompaction is associated with mutations in the HCN4 channel. 25145518 2014