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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNAO1
(D174G)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with involuntary movements
+1 more
GPathogenic
GNAO1
(K271E)
Single nucleotide variant
(missense variant)
Early infantile epileptic encephalopathy with suppression bursts
GUncertain significance