Gene entry
WASHC5
WASH complex subunit 5
- Chromosome
- 8
- Cytoband
- 8q24.13
- Variants (rsID)
- 24
WASHC5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8q24.13). Its official name is “WASH complex subunit 5”. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs370705310Benignsingle nucleotide variantHereditary spastic paraplegia 8
- rs7812319Benignsingle nucleotide variantHereditary spastic paraplegia 8|Ritscher-Schinzel syndrome|Hereditary spastic paraplegia 8|Hereditary spastic paraplegia
- rs72720524Conflicting interpretationssingle nucleotide variantRitscher-Schinzel syndrome|Hereditary spastic paraplegia 8|Hereditary spastic paraplegia 8
- rs80338866Pathogenicsingle nucleotide variantHereditary spastic paraplegia 8|Ritscher-Schinzel syndrome|Hereditary spastic paraplegia 8
- rs80338867Pathogenicsingle nucleotide variantHereditary spastic paraplegia 8|Hereditary spastic paraplegia|Ritscher-Schinzel syndrome|Hereditary spastic paraplegia 8
- rs202015963Uncertain significancesingle nucleotide variant
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.