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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALAS2, APEX2
Single nucleotide variant
(3 prime UTR variant)
not provided
+1 more
GBenign/Likely benign
CXorf49B, CXorf51A
+821 more
Copy number loss
not provided
GPathogenic