RS796053157 SCN2A
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
11
Seizures
benign familial infantile
3
Complex neurodevelopmental disorder
Inborn genetic diseases
Epilepsy of infancy with migrating focal seizures
Genetic developmental and epileptic encephalopathy
SCN2A-related generalized epilepsy with febrile seizures plus
Developmental and epileptic encephalopathy
11
Seizures
benign familial infantile
3
Other Variants in SCN2A