SLC6A2, solute carrier family 6 member 2, 6530

N. diseases: 238; N. variants: 24
Disease: Seizures, Somatosensory ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0422850
Disease: Seizures, Somatosensory
Seizures, Somatosensory 		0.300 Biomarker phenotype CTD_human Genetic deletion of the norepinephrine transporter decreases vulnerability to seizures. 15911120 2005