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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130063254, LOC130063255
+810 more
Copy number gain
See cases
GPathogenic
LOC130063296, TUBB4A
(L13V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance