The association between SLC12A5 (Solute Carrier Family 12 Member 5) and Epilepsy, Idiopathic Generalized 14 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, causative variation, and a susceptibility locus.
Sources4
Clinical variants24
Symptoms11
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.