| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Ritscher-Schinzel syndrome +4 more | |
| | WASHC5, WASHC5-AS1 (Q758E +1 more) | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia +2 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +3 more | GConflicting classifications of pathogenicity |
| | WASHC5, WASHC5-AS1 (T697A +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Hereditary spastic paraplegia +2 more | |
Click to view in NCBI Gene