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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130002822, LOC130002823
+160 more
Copy number loss
See cases
GPathogenic
ABL1, LOC107980440
(P39R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance