The association between SIN3A (SIN3 Transcription Regulator Family Member A) and Chromosome 15q24 Deletion Syndrome is well established and manually curated, with its 2 contributing sources — 2 of them expert-curated — recording pathogenic and likely-pathogenic variants.
Sources2
Clinical variants74
Symptoms54
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.