The association between GNB1 (G Protein Subunit Beta 1) and Intellectual Developmental Disorder, Autosomal Dominant 42 is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and a causative germline mutation.
Sources5
Clinical variants63
Symptoms96
Compounds0
Trials0
Publications12
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.
