RS137854619 SCN5A
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Long QT syndrome 2/3
digenic
Congenital long QT syndrome
Long QT syndrome
Brugada syndrome 1
Cardiac arrhythmia
Cardiovascular phenotype
Atrial fibrillation
Long QT syndrome 2/3
digenic
Congenital long QT syndrome
Long QT syndrome
Brugada syndrome 1
Cardiac arrhythmia
Cardiovascular phenotype
Other Variants in SCN5A