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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC25A38
(P92R)
Single nucleotide variant
(missense variant)
Sideroblastic anemia 2
GLikely pathogenic
SLC25A38
(Y195C)
Single nucleotide variant
(missense variant)
Sideroblastic anemia 2
GUncertain significance