| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | FARS2, LOC126859565 (D142Y) | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia 77 | |
| | LOC126859565, FARS2 (A154V) | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia 77 +1 more | GConflicting classifications of pathogenicity |
| | FARS2, LOC126859565 (H159P) | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia 77 +1 more | GConflicting classifications of pathogenicity |
| | FARS2, LOC126859565 (V174del) | Microsatellite (inframe_deletion +1 more) | Hereditary spastic paraplegia 77 +1 more | |
| | FARS2, LOC126859565 (D184N) | Single nucleotide variant (missense variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary spastic paraplegia 77 +2 more | |
| | FARS2, LOC101927950
+3 more | Deletion | Hereditary spastic paraplegia 77 | |
| | | Single nucleotide variant (missense variant) | See cases +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 77 +2 more | GPathogenic/Likely pathogenic |
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