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FAM237B

family with sequence similarity 237 member B

HCNC Approved Symbol
FAM237B (HGNC:53217)
Genomic Coordinates
: - (7q21.13)
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.

FAM237B - Gene browser | 3billion