The association between SF3B2 (Splicing Factor 3b Subunit 2) and Craniofacial Microsomia 1 is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.
Sources2
Clinical variants7
Symptoms98
Compounds0
Trials0
Publications2
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.