RS796053135 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
West syndrome
Developmental and epileptic encephalopathy
11
Seizures
benign familial infantile
3
West syndrome
Other Variants in SCN2A