RS121918805 SCN1A

Health Risk Chr 2:166002660
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What This Variant Does
"CLNSIG=4
Associated Conditions
Generalized epilepsy with febrile seizures plus
type 1
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Early-infantile DEE
type 2
Migraine
familial hemiplegic
3
Developmental and epileptic encephalopathy 6B
Early-infantile DEE
Generalized epilepsy with febrile seizures plus
type 1
Severe myoclonic epilepsy in infancy
Inborn genetic diseases
Other Variants in SCN1A
rs3812718 rs121918622 rs121918623 rs121917953 rs121917954 rs121917955 rs121917930 rs1574272192 rs121918624 rs121918625
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