SLC6A2, solute carrier family 6 member 2, 6530

N. diseases: 41; N. variants: 2
Disease: Atonic Absence Seizures ×
Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0751123
Disease: Atonic Absence Seizures
Atonic Absence Seizures 		0.300 Biomarker phenotype CTD_human Genetic deletion of the norepinephrine transporter decreases vulnerability to seizures. 15911120 2005