Gene entry
HYLS1
HYLS1 centriolar and ciliogenesis associated
- Chromosome
- 11
- Cytoband
- 11q24.2
- Variants (rsID)
- 4
HYLS1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11q24.2). Its official name is “HYLS1 centriolar and ciliogenesis associated”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs2236681Benignsingle nucleotide variant
- rs104894232Pathogenicsingle nucleotide variantHydrolethalus syndrome|Hydrolethalus syndrome 1
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.