Gene entry
F13B
coagulation factor XIII B chain
- Chromosome
- 1
- Cytoband
- 1q31.3
- Variants (rsID)
- 11
F13B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q31.3). Its official name is “coagulation factor XIII B chain”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs6003Benignsingle nucleotide variantVenous thrombosis, susceptibility to|Factor XIII, b subunit, deficiency of
- rs149088047Conflicting interpretationssingle nucleotide variantFactor XIII, b subunit, deficiency of
- rs17514253Uncertain significancesingle nucleotide variantFactor XIII, b subunit, deficiency of
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.