Gene entry
SERPINF1
serpin family F member 1
- Chromosome
- 17
- Cytoband
- 17p13.3
- Variants (rsID)
- 14
SERPINF1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p13.3). Its official name is “serpin family F member 1”. The reference table lists 14 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs1136287Benignsingle nucleotide variantOsteogenesis imperfecta type 6|Osteogenesis imperfecta
- rs34063250Benignsingle nucleotide variantOsteogenesis imperfecta type 6
- rs8074840Benignsingle nucleotide variantOsteogenesis imperfecta type 6
- rs9913583Benignsingle nucleotide variantOsteogenesis Imperfecta, Recessive|Osteogenesis imperfecta
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.