Gene entry
C5
complement C5
- Chromosome
- 9
- Cytoband
- 9q33.2
- Variants (rsID)
- 24
C5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q33.2). Its official name is “complement C5”. The reference table lists 24 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs10985112Benignsingle nucleotide variant
- rs17611Benignsingle nucleotide variant
- rs56040400Likely benignsingle nucleotide variantEculizumab, poor response to
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.