SLC6A2, solute carrier family 6 member 2, 6530

N. diseases: 238; N. variants: 24
Disease: Familial (FPAH) ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 GeneticVariation disease BEFREE Familial orthostatic tachycardia due to norepinephrine transporter deficiency. 11458707 2001