RS746413385 SCN1A
Upload your DNA to see your genotype for this variant.
Associated Conditions
Migraine
familial hemiplegic
3
Developmental and epileptic encephalopathy 6B
Severe myoclonic epilepsy in infancy
Generalized epilepsy with febrile seizures plus
type 2
Early-infantile DEE
Migraine
familial hemiplegic
3
Developmental and epileptic encephalopathy 6B
Severe myoclonic epilepsy in infancy
Generalized epilepsy with febrile seizures plus
type 2
Other Variants in SCN1A