RS121917935 SCN1A

Health Risk Chr 2:166054660
Upload your DNA to see your genotype for this variant.
Associated Conditions
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Seizure
Generalized epilepsy with febrile seizures plus
type 2
Developmental and epileptic encephalopathy 6B
Febrile seizures
familial
3a
Autosomal dominant epilepsy
Early-infantile DEE
Early-infantile DEE
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Seizure
Other Variants in SCN1A
rs3812718 rs121918622 rs121918623 rs121917953 rs121917954 rs121917955 rs121917930 rs1574272192 rs121918624 rs121918625
Ask Dr. Hemsworth about this variant