Gene entry
FANCB
FA complementation group B
- Chromosome
- X
- Cytoband
- Xp22.2
- Variants (rsID)
- 25
FANCB is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp22.2). Its official name is “FA complementation group B”. The reference table lists 25 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs146157131Conflicting interpretationssingle nucleotide variantFanconi anemia
- rs200161949Conflicting interpretationssingle nucleotide variantFanconi anemia
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.
