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C17orf100

chromosome 17 open reading frame 100

HCNC Approved Symbol
C17orf100 (HGNC:34494)
Genomic Coordinates
: - (17p13.1)
Synonyms
LOC388327
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.