RS797044951 GNAO1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Neurodevelopmental disorder with involuntary movements
Developmental delay
Abnormality of the nervous system
GNAO1-related developmental delay-seizures-movement disorder spectrum
Early-infantile DEE
Developmental and epileptic encephalopathy
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Neurodevelopmental disorder with involuntary movements
Inborn genetic diseases
Neurodevelopmental disorder with involuntary movements
Developmental delay
Abnormality of the nervous system
GNAO1-related developmental delay-seizures-movement disorder spectrum
Early-infantile DEE
Other Variants in GNAO1