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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129992625, SRP72
(G7E)
Single nucleotide variant
(missense variant +1 more)
Autosomal dominant aplasia and myelodysplasia
+2 more
GConflicting classifications of pathogenicity
LOC129992625, SRP72
(G8E)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity