Gene entry

FGF9

fibroblast growth factor 9

Chromosome: 13
Cytoband: 13q12.11
Variants (rsID): 8

FGF9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q12.11). Its official name is “fibroblast growth factor 9”. The reference table lists 8 variants (rsID) for this gene.

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Clinically classified variants

2 reference-table entries with clinical significance.

rs9509841Benignsingle nucleotide variantMultiple synostoses syndrome 3
rs9509843Benignsingle nucleotide variantMultiple synostoses syndrome 3

Other listed variants

rs9509833
rs9580187
rs12427696
rs17070605
rs74499014
rs76152173

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.