Gene entry
C6
complement C6
- Chromosome
- 5
- Cytoband
- 5p13.1
- Variants (rsID)
- 30
C6 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 C6”. The reference table lists 30 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs1801033Benignsingle nucleotide variant
- rs76202909Conflicting interpretationssingle nucleotide variantC6 deficiency, subtotal|Complement component 6 deficiency
- rs142881576Pathogenicsingle nucleotide variantComplement component 6 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.