RS398123588 SCN1A

Health Risk Chr 2:166039436
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant epilepsy
Seizure
Generalized epilepsy with febrile seizures plus
type 2
Severe myoclonic epilepsy in infancy
SCN1A-related disorder
Early-infantile DEE
Autosomal dominant epilepsy
Seizure
Generalized epilepsy with febrile seizures plus
type 2
Severe myoclonic epilepsy in infancy
SCN1A-related disorder
Early-infantile DEE
Other Variants in SCN1A
rs3812718 rs121918622 rs121918623 rs121917953 rs121917954 rs121917955 rs121917930 rs1574272192 rs121918624 rs121918625
Ask Dr. Hemsworth about this variant