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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNA1A
(R192W)
Single nucleotide variant
(missense variant)
Episodic ataxia type 2
+2 more
GConflicting classifications of pathogenicity
NOP56
(S151T)
Single nucleotide variant
(missense variant +1 more)
Mild global developmental delay
+1 more
GUncertain significance