RS121917923 SCN1A
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What This Variant Does
"CLNSIG=5
Associated Conditions
Severe myoclonic epilepsy in infancy
Severe myoclonic epilepsy in infancy
Developmental and epileptic encephalopathy
6A
Severe myoclonic epilepsy in infancy
Severe myoclonic epilepsy in infancy
Severe myoclonic epilepsy in infancy
Developmental and epileptic encephalopathy
6A
Severe myoclonic epilepsy in infancy
Other Variants in SCN1A