Gene entry
FOXN1
forkhead box N1
- Chromosome
- 17
- Cytoband
- 17q11.2
- Variants (rsID)
- 17
FOXN1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q11.2). Its official name is “forkhead box N1”. The reference table lists 17 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs12449554Benignsingle nucleotide variantT-cell immunodeficiency, congenital alopecia, and nail dystrophy
- rs3744635Benignsingle nucleotide variantT-cell immunodeficiency, congenital alopecia, and nail dystrophy
- rs614434Benignsingle nucleotide variantT-cell immunodeficiency, congenital alopecia, and nail dystrophy
- rs137872361Conflicting interpretationssingle nucleotide variantT-cell immunodeficiency, congenital alopecia, and nail dystrophy
- rs144301161Conflicting interpretationssingle nucleotide variantT-cell immunodeficiency, congenital alopecia, and nail dystrophy
- rs34814444Conflicting interpretationssingle nucleotide variantT-cell immunodeficiency, congenital alopecia, and nail dystrophy
- rs73278523Likely benignsingle nucleotide variantT-cell immunodeficiency, congenital alopecia, and nail dystrophy
- rs181483148Uncertain significancesingle nucleotide variantT-cell immunodeficiency, congenital alopecia, and nail dystrophy
- rs200053524Uncertain significancesingle nucleotide variantT-cell immunodeficiency, congenital alopecia, and nail dystrophy
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.