RS797044878 GNAO1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Neurodevelopmental disorder with involuntary movements
Developmental and epileptic encephalopathy
17
Early-infantile DEE
Developmental and epileptic encephalopathy
17
Early-infantile DEE
Inborn genetic diseases
Neurodevelopmental disorder with involuntary movements
Developmental and epileptic encephalopathy
17
Early-infantile DEE
Developmental and epileptic encephalopathy
17
Other Variants in GNAO1