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C18orf63

chromosome 18 open reading frame 63

HCNC Approved Symbol
C18orf63 (HGNC:40037)
Genomic Coordinates
: - (18q22.3)
Synonyms
DKFZP781G0119
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.