RS796052653 KCNQ2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
7
Seizures
benign familial neonatal
1
Inborn genetic diseases
Early-infantile DEE
Developmental and epileptic encephalopathy
7
Seizures
benign familial neonatal
1
Inborn genetic diseases
Early-infantile DEE
Other Variants in KCNQ2