RS118192208 KCNQ2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Seizures
benign familial neonatal
1
Inborn genetic diseases
Early-infantile DEE
Seizures
benign familial neonatal
1
Early-infantile DEE
Seizures
benign familial neonatal
1
Inborn genetic diseases
Early-infantile DEE
Seizures
Population Frequencies
gnomAD ALL
0%
Other Variants in KCNQ2