The association between RAB3GAP1 (RAB3 GTPase Activating Protein Catalytic Subunit 1) and Martsolf Syndrome 2 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording a known molecular basis and pathogenic variants.
Sources3
Clinical variants13
Symptoms33
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.