RS776913277 BRAT1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neonatal-onset encephalopathy with rigidity and seizures
Neurodevelopmental disorder with cerebellar atrophy and with or without seizures
Inborn genetic diseases
BRAT1-related disorder
Neonatal-onset encephalopathy with rigidity and seizures
Neurodevelopmental disorder with cerebellar atrophy and with or without seizures
Inborn genetic diseases
BRAT1-related disorder
Other Variants in BRAT1