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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAPRIN1
(P512L)
Single nucleotide variant
(missense variant)
Cerebellar ataxia
+2 more
GConflicting classifications of pathogenicity
VPS39
Single nucleotide variant
(splice acceptor variant)
Cerebellar ataxia
GUncertain significance