RS762251339 KCNT1

Health Risk Chr 9:135757213
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Associated Conditions
Inborn genetic diseases
Developmental and epileptic encephalopathy
14
Autosomal dominant nocturnal frontal lobe epilepsy 5
Inborn genetic diseases
Developmental and epileptic encephalopathy
14
Autosomal dominant nocturnal frontal lobe epilepsy 5
Other Variants in KCNT1
rs397515402 rs397515403 rs397515404 rs370521183 rs397515405 rs397515406 rs397515407 rs886044717 rs587777264 rs547714141
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