RS16969925 SCN1B
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What This Variant Does
"CLNSIG=5
Associated Conditions
Atrial fibrillation
familial
13
Generalized epilepsy with febrile seizures plus
type 1
Developmental and epileptic encephalopathy
52
Brugada syndrome 5
Cardiovascular phenotype
SCN1B-related disorder
Atrial fibrillation
familial
13
Generalized epilepsy with febrile seizures plus
type 1
Other Variants in SCN1B