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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBC1D1, LOC126807034
(R327K)
Single nucleotide variant
(missense variant)
not provided
GBenign/Likely benign
ABLIM2, ACOX3
+226 more
Copy number gain
See cases
GPathogenic