RS74315392 KCNQ2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Developmental and epileptic encephalopathy
7
Seizures
benign familial neonatal
2
Early-infantile DEE
Inborn genetic diseases
Developmental and epileptic encephalopathy
7
Seizures
benign familial neonatal
1
Early-infantile DEE
Developmental and epileptic encephalopathy
7
Other Variants in KCNQ2