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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDYN, PDYN-AS1
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
PDYN-AS1, PDYN
(M146L)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 23
+2 more
GBenign/Likely benign
PDYN, PDYN-AS1
(R25Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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