RS794726730 SCN1A

Health Risk Chr 2:166042334
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What This Variant Does
"CLNSIG=5
Associated Conditions
Severe myoclonic epilepsy in infancy
Generalized epilepsy with febrile seizures plus
type 2
Developmental and epileptic encephalopathy
1
Autosomal dominant epilepsy
Inborn genetic diseases
SCN1A-related disorder
Early-infantile DEE
Severe myoclonic epilepsy in infancy
Generalized epilepsy with febrile seizures plus
type 2
Developmental and epileptic encephalopathy
1
Autosomal dominant epilepsy
Other Variants in SCN1A
rs3812718 rs121918622 rs121918623 rs121917953 rs121917954 rs121917955 rs121917930 rs1574272192 rs121918624 rs121918625
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