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Items: 3

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
SAMD9
(I732S)
Single nucleotide variant
(missense variant)
See cases
GLikely pathogenic
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