RS137854604 SCN5A
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What This Variant Does
"A publication has reported that the minor (and quite rare) T allele of rs137854604 was seen in a 39-...
Associated Conditions
Ventricular fibrillation
paroxysmal familial
type 1
Brugada syndrome 1
Cardiovascular phenotype
Cardiac arrhythmia
8 conditions
Brugada syndrome
Long QT syndrome 3
Ventricular fibrillation
paroxysmal familial
type 1
Brugada syndrome 1
Cardiovascular phenotype
Cardiac arrhythmia
Other Variants in SCN5A