SLC2A9, solute carrier family 2 member 9, 56606

N. diseases: 74; N. variants: 389
Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6283
rs6283
Entrez Id: 1816;56606
Gene Symbol: DRD5;SLC2A9
DRD5;SLC2A9
CUI: C0030567
Disease:
Parkinson Disease 		0.010 GeneticVariation BEFREE It suggests that DRD5 T978C polymorphism is not associated with the susceptibility to PD, nor with the risk of developing motor fluctuations in PD. 11445276 2001