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FAM98C

family with sequence similarity 98 member C

HCNC Approved Symbol
FAM98C (HGNC:27119)
Genomic Coordinates
: - (19q13.2)
Synonyms
FLJ44669
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.

FAM98C - Gene browser | 3billion