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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SAMD9
(P1555R)
Single nucleotide variant
(missense variant)
Myelodysplasia
GUncertain significance
SAMD9
(A1338fs)
Duplication
(frameshift variant)
Myelodysplasia
GPathogenic