RS869312939 GNAO1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Developmental and epileptic encephalopathy
Early-infantile DEE
Developmental and epileptic encephalopathy
17
Neurodevelopmental disorder with involuntary movements
Inborn genetic diseases
Developmental and epileptic encephalopathy
Early-infantile DEE
Developmental and epileptic encephalopathy
17
Neurodevelopmental disorder with involuntary movements
Other Variants in GNAO1