Gene entry
FGF8
fibroblast growth factor 8
- Chromosome
- 10
- Cytoband
- 10q24.32
- Variants (rsID)
- 4
FGF8 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q24.32). Its official name is “fibroblast growth factor 8”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs137852660Conflicting interpretationssingle nucleotide variantHypogonadotropic hypogonadism 6 with or without anosmia
- rs137852664Conflicting interpretationssingle nucleotide variantHypogonadotropic hypogonadism 6 with or without anosmia|Holoprosencephaly 1
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.