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SNX19

sorting nexin 19

HCNC Approved Symbol
SNX19 (HGNC:21532)
Genomic Coordinates
: - (11q24.3-q25)
Synonyms
KIAA0254, CHET8
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there are 3 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

SNX19 - Gene browser | 3billion