| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130006506, NARS2 (E155A +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | NARS2, LOC130006506 (M151L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
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