| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +6 more | GConflicting classifications of pathogenicity |
| | LOC126806583, KIF1A (R1195H +8 more) | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia +4 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene