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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDAN1
(P1130L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
CDAN1
(R1042W)
Single nucleotide variant
(missense variant)
Anemia, congenital dyserythropoietic, type 1a
+1 more
GPathogenic/Likely pathogenic
CDAN1
(P672L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
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