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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC88C
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
CCDC88C
Single nucleotide variant
(synonymous variant)
Spinocerebellar ataxia type 40
+2 more
GBenign/Likely benign