Gene entry
C9
complement C9
- Chromosome
- 5
- Cytoband
- 5p13.1
- Variants (rsID)
- 18
C9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5p13.1). Its official name is “complement C9”. The reference table lists 18 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs476569Benignsingle nucleotide variant
- rs696763Benignsingle nucleotide variant
- rs34882957Likely benignsingle nucleotide variantAge related macular degeneration 15
- rs34000044Pathogenicsingle nucleotide variantComplement component 9 deficiency
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.