RS749205120 KCNQ3
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Seizures
benign familial neonatal
2
Benign neonatal seizures
See cases
Seizure
Inborn genetic diseases
Seizures
benign familial neonatal
2
Benign neonatal seizures
See cases
Seizure
Other Variants in KCNQ3