Gene entry
CFP
complement factor properdin
- Chromosome
- X
- Cytoband
- Xp11.23
- Variants (rsID)
- 7
CFP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp11.23). Its official name is “complement factor properdin”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs1048118Benignsingle nucleotide variant
- rs132630259Pathogenicsingle nucleotide variantProperdin deficiency, type II
- rs132630261Pathogenicsingle nucleotide variantProperdin deficiency, type III
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.