| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | FDX2, FDX2-ZGLP1 (P144L +1 more) | Single nucleotide variant (missense variant) | Inborn mitochondrial myopathy | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression +1 more | GPathogenic/Likely pathogenic |
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