brugada syndrome Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
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Genes

4 genes associated with the disease brugada syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
GPD1L glycerol-3-phosphate dehydrogenase 1-like
SCN1B sodium channel, voltage gated, type I beta subunit
SCN2B sodium channel, voltage gated, type II beta subunit
SCN5A sodium channel, voltage gated, type V alpha subunit