RS104894718 SCN1B
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What This Variant Does
"[OMIM:?]
Associated Conditions
Generalized epilepsy with febrile seizures plus
type 1
Atrial fibrillation
familial
13
Brugada syndrome 5
Developmental and epileptic encephalopathy
52
Cardiovascular phenotype
SCN1B-related disorder
Generalized epilepsy with febrile seizures plus
type 1
Atrial fibrillation
familial
13
Other Variants in SCN1B