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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GBA2
(W603R)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+3 more
GUncertain significance
GBA2
(N482H)
Single nucleotide variant
(missense variant)
Cerebellar ataxia
+4 more
GUncertain significance