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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PEX10
(K17R)
Single nucleotide variant
(missense variant +1 more)
Peroxisome biogenesis disorder 6A (Zellweger)
+1 more
GUncertain significance
CCDC27, MIR200B
+79 more
Copy number loss
Primary dilated cardiomyopathy
+2 more
GPathogenic