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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SH2B3
(Q240P +1 more)
Single nucleotide variant
(missense variant)
Primary myelofibrosis
GUncertain significance
SH2B3
(E321fs +1 more)
Duplication
(frameshift variant)
Primary myelofibrosis
GLikely pathogenic