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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SH2B3
(S101fs +1 more)
Deletion
(frameshift variant)
not provided
GUncertain significance
SH2B3
(E198K +1 more)
Single nucleotide variant
(missense variant)
Primary myelofibrosis
+3 more
GUncertain significance