RS764115258 SCN8A
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Associated Conditions
Cognitive impairment with or without cerebellar ataxia
Seizures
benign familial infantile
5
Developmental and epileptic encephalopathy
13
Inborn genetic diseases
Early-infantile DEE
Myoclonus
familial
2
Cognitive impairment with or without cerebellar ataxia
Seizures
benign familial infantile
5
Other Variants in SCN8A