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Is Brugada Syndrome Genetic?
- Heritability
- ~100%
- Inheritance
- autosomal-dominant
- Key genes
- SCN5A
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A channelopathy causing life-threatening arrhythmias. About 20–30% of cases carry SCN5A mutations. Penetrance is highly variable.
How Genetic Is Brugada Syndrome?
Brugada Syndrome has a strong genetic basis. Research estimates heritability at approximately 100%, meaning genetic factors account for the majority of variation in whether individuals develop this condition.
Key genes associated with Brugada Syndrome: SCN5A. Variants in these genes have been identified through genome-wide association studies (GWAS) and clinical research as influencing susceptibility or severity.
Source: MedlinePlus Genetics
Does Family History Matter for Brugada Syndrome?
Yes — family history is one of the strongest predictors of Brugada Syndrome. If a first-degree relative (parent, sibling, or child) has been diagnosed, your own risk may be significantly elevated. Discussing your family history with a healthcare provider or genetic counsellor is strongly recommended.
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