Gene entry
FOXC1
forkhead box C1
- Chromosome
- 6
- Cytoband
- 6p25.3
- Variants (rsID)
- 5
FOXC1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p25.3). Its official name is “forkhead box C1”. The reference table lists 5 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs79691946Benignsingle nucleotide variantAnterior segment dysgenesis 3|Axenfeld-Rieger syndrome type 3
- rs121909338Conflicting interpretationssingle nucleotide variantAxenfeld-Rieger syndrome type 3
- rs104893951Pathogenicsingle nucleotide variantAxenfeld-Rieger syndrome type 3
- rs886039568Pathogenicsingle nucleotide variantAxenfeld-Rieger syndrome type 3
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.