Gene entry
FGD1
FYVE, RhoGEF and PH domain containing 1
- Chromosome
- X
- Cytoband
- Xp11.22
- Variants (rsID)
- 8
FGD1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp11.22). Its official name is “FYVE, RhoGEF and PH domain containing 1”. The reference table lists 8 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs1126744Benignsingle nucleotide variantHistory of neurodevelopmental disorder
- rs2230265Benignsingle nucleotide variantAarskog syndrome
- rs28935497Pathogenicsingle nucleotide variantAarskog syndrome
- rs398124159Uncertain significancesingle nucleotide variantInborn genetic diseases
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.