Brugada syndrome Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A heart conduction disease that is characterized by abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac death. (Human Disease Ontology, DOID_0050451)
External Link http://purl.bioontology.org/ontology/SNOMEDCT/418818005
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Genes

2 genes associated with the Brugada syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
SCN5A sodium channel, voltage gated, type V alpha subunit