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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDAN1
(A887V)
Single nucleotide variant
(missense variant)
Anemia, congenital dyserythropoietic, type 1a
GUncertain significance
CDAN1
(M588T)
Single nucleotide variant
(missense variant)
Anemia, congenital dyserythropoietic, type 1a
+1 more
GUncertain significance