The association between SLC12A6 (Solute Carrier Family 12 Member 6) and Charcot-Marie-Tooth Disease, Axonal, Type 2ii is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.
Sources4
Clinical variants32
Symptoms46
Compounds0
Trials0
Publications5
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.