MGC1346, SF3b14b, INI, bK223H9.2, Rds3, SAP14b, SF3B7
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 is 1 patient* with variant(s) predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.