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FRG2C

FSHD region gene 2 family member C

HCNC Approved Symbol
FRG2C (HGNC:33626)
Genomic Coordinates
: - (3p12.3)
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.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

FRG2C - Gene browser | 3billion