RS886039494 GNAO1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neurodevelopmental disorder with involuntary movements
Inborn genetic diseases
Movement disorder
Developmental and epileptic encephalopathy
17
GNAO1-related disorder
Early-infantile DEE
Neurodevelopmental disorder with involuntary movements
Neurodevelopmental disorder with involuntary movements
Inborn genetic diseases
Movement disorder
Developmental and epileptic encephalopathy
17
GNAO1-related disorder
Early-infantile DEE
Other Variants in GNAO1