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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MIPEP, PCOTH
(A14T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
C1QTNF9, C1QTNF9B
+6 more
Copy number loss
Cardiomyopathy
+2 more
GPathogenic