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FGF22

fibroblast growth factor 22

HCNC Approved Symbol
FGF22 (HGNC:3679)
Genomic Coordinates
19:639,879 - 644,373 (19p13.3)
Synonyms
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there are 3 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

FGF22 - Gene browser | 3billion