Gene entry
FSCN2
fascin actin-bundling protein 2, retinal
- Chromosome
- 17
- Cytoband
- 17q25.3
- Variants (rsID)
- 10
FSCN2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q25.3). Its official name is “fascin actin-bundling protein 2, retinal”. The reference table lists 10 variants (rsID) for this gene.
Clinically classified variants
3 reference-table entries with clinical significance.
- rs143796236Benignsingle nucleotide variant
- rs186367879Benignsingle nucleotide variant
- rs181961770Uncertain significancesingle nucleotide variant
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.