Variant (rsID / SNP)
rs73278523
rs73278523 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOXN1. Location: chromosome 17, position 26,864,264. Clinical significance in the table: Likely benign.
Reference-table entries
FOXN1Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:26864264
- Cytoband
- 17q11.2
- HGVS
- NM_001369369.1(FOXN1):c.1757G>A (p.Cys586Tyr)
- Allele change
- Missense_C586Y
Associated conditions / phenotypes
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.