RS745590718 KCNT1

Health Risk Chr 9:135784773
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Associated Conditions
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy 5
Developmental and epileptic encephalopathy
14
Inborn genetic diseases
Autosomal dominant nocturnal frontal lobe epilepsy 5
Developmental and epileptic encephalopathy
14
Other Variants in KCNT1
rs397515402 rs397515403 rs397515404 rs370521183 rs397515405 rs397515406 rs397515407 rs886044717 rs587777264 rs547714141
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