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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FDX2, FDX2-ZGLP1
+1 more
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GBenign
FDX2, FDX2-ZGLP1
Single nucleotide variant
(synonymous variant +1 more)
Mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy
+2 more
GBenign