The association between COL6A2 (Collagen Type VI Alpha 2 Chain) and Ullrich Congenital Muscular Dystrophy 1a is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording likely-pathogenic variants and a causative germline mutation.
Sources3
Clinical variants75
Symptoms89
Compounds0
Trials0
Publications22
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.