Gene entry
FOXG1
forkhead box G1
- Chromosome
- 14
- Cytoband
- 14q12
- Variants (rsID)
- 13
FOXG1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q12). Its official name is “forkhead box G1”. The reference table lists 13 variants (rsID) for this gene.
Clinically classified variants
11 reference-table entries with clinical significance.
- rs375378714Benignsingle nucleotide variantRett syndrome, congenital variant|History of neurodevelopmental disorder|FOXG1 disorder
- rs796052455Benignsingle nucleotide variantRett syndrome, congenital variant
- rs141088742Conflicting interpretationssingle nucleotide variantRett syndrome, congenital variant
- rs796052472Conflicting interpretationssingle nucleotide variantRett syndrome, congenital variant
- rs398124203Likely benignsingle nucleotide variantRett syndrome, congenital variant|FOXG1 disorder
- rs148410675Likely pathogenicsingle nucleotide variant
- rs121913678Pathogenicsingle nucleotide variantRett syndrome, congenital variant
- rs267606827Pathogenicsingle nucleotide variantRett syndrome, congenital variant
- rs587783635PathogenicDeletionRett syndrome, congenital variant
- rs587783643Pathogenicsingle nucleotide variantRett syndrome, congenital variant|FOXG1 disorder
- rs786205006Pathogenicsingle 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.