Gene entry
F10
coagulation factor X
- Chromosome
- 13
- Cytoband
- 13q34
- Variants (rsID)
- 12
F10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q34). Its official name is “coagulation factor X”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs3093253Benignsingle nucleotide variantFactor X deficiency|Factor VII deficiency
- rs5960Benignsingle nucleotide variantHereditary factor X deficiency disease
- rs104894392Pathogenicsingle nucleotide variantFactor X 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.