Gene entry
FPR1
formyl peptide receptor 1
- Chromosome
- 19
- Cytoband
- 19q13.41
- Variants (rsID)
- 7
FPR1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.41). Its official name is “formyl peptide receptor 1”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs28930680Benignsingle nucleotide variantGingival disorder
- rs5030878Benignsingle nucleotide variantGingival disorder
- rs78488639Benignsingle nucleotide variantGingival disorder
- rs186613919Uncertain significancesingle nucleotide variantGingival disorder
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.