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C19orf67

chromosome 19 open reading frame 67

HCNC Approved Symbol
C19orf67 (HGNC:34354)
Genomic Coordinates
: - (19p13.12)
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.

C19orf67 - Gene browser | 3billion