RS74315391 KCNQ2

Health Risk Chr 20:63444730
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What This Variant Does
"[OMIM:?]
Associated Conditions
Seizures
benign familial neonatal
1
and/or myokymia
Inborn genetic diseases
Developmental and epileptic encephalopathy
7
Complex neurodevelopmental disorder
Seizure
Early-infantile DEE
Seizures
benign familial neonatal
1
and/or myokymia
Inborn genetic diseases
Other Variants in KCNQ2
rs28939683 rs74315390 rs28939684 rs267607198 rs74315392 rs118192244 rs118192200 rs118192217 rs118192218 rs118192219
Ask Dr. Hemsworth about this variant