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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SKI
(G116E)
Single nucleotide variant
(missense variant)
Shprintzen-Goldberg syndrome
GPathogenic/Likely pathogenic
SKI
(A579T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
CCDC27, MIR200B
+79 more
Copy number loss
Primary dilated cardiomyopathy
+2 more
GPathogenic
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