Gene entry
C7
complement C7
- Chromosome
- 5
- Cytoband
- 5p13.1
- Variants (rsID)
- 19
C7 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 C7”. The reference table lists 19 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs121964921Pathogenicsingle nucleotide variantComplement component 7 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.