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FAM186A

family with sequence similarity 186 member A

HCNC Approved Symbol
FAM186A (HGNC:26980)
Genomic Coordinates
: - (12q13.12)
Synonyms
LOC121006
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 7 patients* with variant(s) predicted to be damaging.*3 of the patients have been diagnosed with a variant in another gene.

FAM186A - Gene browser | 3billion