Gene entry
FKBP10
FKBP prolyl isomerase 10
- Chromosome
- 17
- Cytoband
- 17q21.2
- Variants (rsID)
- 9
FKBP10 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q21.2). Its official name is “FKBP prolyl isomerase 10”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs34764749Conflicting interpretationssingle nucleotide variantOsteogenesis imperfecta type 11
- rs61749879Conflicting interpretationssingle nucleotide variantOsteogenesis imperfecta type 11|Osteogenesis imperfecta
- rs869320752PathogenicDeletionBruck syndrome 1
- rs141387386Uncertain significancesingle nucleotide variantOsteogenesis imperfecta type 11
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.