RS397515404 KCNT1

Health Risk Chr 9:135768848
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What This Variant Does
"CLNSIG=5
Associated Conditions
Developmental and epileptic encephalopathy
14
Autosomal dominant nocturnal frontal lobe epilepsy 5
Inborn genetic diseases
Seizure
KCNT1-related disorder
15
Inborn genetic diseases
Developmental and epileptic encephalopathy
14
Autosomal dominant nocturnal frontal lobe epilepsy 5
Inborn genetic diseases
Seizure
KCNT1-related disorder
15
Other Variants in KCNT1
rs397515402 rs397515403 rs370521183 rs397515405 rs397515406 rs397515407 rs886044717 rs587777264 rs547714141 rs143355299
Ask Dr. Hemsworth about this variant