RS151272083 KCNT1
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What This Variant Does
"CLNSIG=4
Associated Conditions
Developmental and epileptic encephalopathy
14
Autosomal dominant nocturnal frontal lobe epilepsy 5
Inborn genetic diseases
KCNT1-related disorder
Ovarian serous cystadenocarcinoma
Thyroid cancer
nonmedullary
1
Developmental and epileptic encephalopathy
14
Autosomal dominant nocturnal frontal lobe epilepsy 5
Inborn genetic diseases
KCNT1-related disorder
Ovarian serous cystadenocarcinoma
Other Variants in KCNT1