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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC37A4
(N27K)
Single nucleotide variant
(missense variant +1 more)
Glycogen storage disease, type I
+1 more
GConflicting classifications of pathogenicity
DGCR8, ESS2
+45 more
Copy number loss
Ear malformation
+13 more
GPathogenic