| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FARS2, LOC129995672
+1 more | Duplication (genic upstream transcript variant +2 more) | not provided +2 more | |
| | FARS2, LOC126859565 (A166V) | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia 77 +2 more | GConflicting classifications of pathogenicity |
| | FARS2, LOC126859565 (L172P) | Single nucleotide variant (missense variant +1 more) | Combined oxidative phosphorylation defect type 14 +1 more | |
Click to view in NCBI Gene