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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129389795, LOC129389796
+636 more
Copy number gain
See cases
GPathogenic
GRB10
(P36L)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GBenign