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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FDX2, FDX2-ZGLP1
(P144L +1 more)
Single nucleotide variant
(missense variant)
Inborn mitochondrial myopathy
GLikely pathogenic
FDX2-ZGLP1, FDX2
(M4L)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity