| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | NARS2-related primary mitochondrial disorder | |
| | LOC130006506, NARS2 (N154D +1 more) | Single nucleotide variant (missense variant) | Combined oxidative phosphorylation defect type 24 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not provided | |
| | | Copy number gain | not provided | |
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