Gene entry
PFN1
profilin 1
- Chromosome
- 17
- Cytoband
- 17p13.2
- Variants (rsID)
- 1
PFN1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p13.2). Its official name is “profilin 1”. The reference table lists 1 variant (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs140547520Uncertain significancesingle nucleotide variantAmyotrophic lateral sclerosis type 18
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.