Gene entry
FXN
frataxin
- Chromosome
- 9
- Cytoband
- 9q21.11
- Variants (rsID)
- 11
FXN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q21.11). Its official name is “frataxin”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs104894107Conflicting interpretationssingle nucleotide variantFriedreich ataxia
- rs141858334Conflicting interpretationssingle nucleotide variantCardiovascular phenotype
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.
