The association between SMC1A (Structural Maintenance Of Chromosomes 1A) and Rett Syndrome, Congenital Variant is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording pathogenic variants and a causative germline mutation.
Sources3
Clinical variants1
Symptoms133
Compounds0
Trials0
Publications1
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.