RS137854602 SCN5A
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Brugada syndrome 1
Primary familial hypertrophic cardiomyopathy
Cardiac arrhythmia
Cardiovascular phenotype
Brugada syndrome (shorter-than-normal QT interval)
Brugada syndrome 1
Primary familial hypertrophic cardiomyopathy
Cardiac arrhythmia
Cardiovascular phenotype
Brugada syndrome (shorter-than-normal QT interval)
Other Variants in SCN5A