RS886041339 KCNQ2

Health Risk Chr 20:63424194
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What This Variant Does
"CLNSIG=5
Associated Conditions
Seizures
benign familial neonatal
1
Developmental and epileptic encephalopathy
7
Early-infantile DEE
Seizures
benign familial neonatal
1
Inborn genetic diseases
Early-infantile DEE
Seizures
benign familial neonatal
1
Developmental and epileptic encephalopathy
Other Variants in KCNQ2
rs28939683 rs74315390 rs28939684 rs74315391 rs267607198 rs74315392 rs118192244 rs118192200 rs118192217 rs118192218
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