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FAM170B

family with sequence similarity 170 member B

HCNC Approved Symbol
FAM170B (HGNC:19736)
Genomic Coordinates
: - (10q11.23)
Synonyms
AC084727.4, C10orf73
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.

FAM170B - Gene browser | 3billion