brugada syndrome Gene Set

Dataset GWASdb SNP-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)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/DOID:0050451
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Genes

3 genes associated with the disease brugada syndrome in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
SCN10A sodium channel, voltage gated, type X alpha subunit 2.7698
SCN5A sodium channel, voltage gated, type V alpha subunit 1.78856
TBX5 T-box 5 0.565297