RS121917753 SCN2A
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What This Variant Does
"[OMIM:?]
Associated Conditions
Seizures
benign familial infantile
3
Complex neurodevelopmental disorder
Developmental and epileptic encephalopathy
11
Benign familial infantile epilepsy
benign sporadic infantile epilepsy
Developmental and epileptic encephalopathy
11
Complex neurodevelopmental disorder
Episodic ataxia
type 9
Seizures
benign familial infantile
Other Variants in SCN2A