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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SAMD9
(E861fs)
Insertion
(frameshift variant)
Monosomy 7 myelodysplasia and leukemia syndrome 2
+1 more
GUncertain significance
SAMD9
(D805G)
Single nucleotide variant
(missense variant)
MIRAGE syndrome
GLikely pathogenic