RS397515407 KCNT1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant nocturnal frontal lobe epilepsy 5
Developmental and epileptic encephalopathy
14
Epilepsy syndrome
KCNT1-related disorder
Seizure
Childhood-onset epilepsy syndrome
Autosomal dominant nocturnal frontal lobe epilepsy 5
Developmental and epileptic encephalopathy
14
Epilepsy syndrome
KCNT1-related disorder
Seizure
Childhood-onset epilepsy syndrome
Other Variants in KCNT1