RS776446104 SCN8A
Upload your DNA to see your genotype for this variant.
Associated Conditions
Cognitive impairment with or without cerebellar ataxia
Seizures
benign familial infantile
5
Myoclonus
familial
2
Developmental and epileptic encephalopathy
13
Early-infantile DEE
Cognitive impairment with or without cerebellar ataxia
Seizures
benign familial infantile
5
Myoclonus
Other Variants in SCN8A