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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SAMD9
(L1511S)
Single nucleotide variant
(missense variant)
Monosomy 7 myelodysplasia and leukemia syndrome 2
GUncertain significance
SAMD9
(E1046K)
Single nucleotide variant
(missense variant)
Monosomy 7 myelodysplasia and leukemia syndrome 2
GUncertain significance
SAMD9
(S502R)
Single nucleotide variant
(missense variant)
Monosomy 7 myelodysplasia and leukemia syndrome 2
GUncertain significance
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