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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS16
(R187*)
Single nucleotide variant
(nonsense)
not provided
+1 more
GConflicting classifications of pathogenicity
PTPRA, VPS16
Single nucleotide variant
(intron variant)
Dystonia 30
GUncertain significance