RS587777721 SCN8A
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
13
developmental delay with seizures
Inborn genetic diseases
Complex neurodevelopmental disorder
Early-infantile DEE
Developmental and epileptic encephalopathy
13
Early-infantile DEE
Developmental and epileptic encephalopathy
13
developmental delay with seizures
Inborn genetic diseases
Complex neurodevelopmental disorder
Early-infantile DEE
Other Variants in SCN8A