SLC2A9, solute carrier family 2 member 9, 56606

N. diseases: 74; N. variants: 389
Disease: Hyperuricemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6855911
rs6855911
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0740394
Disease:
Hyperuricemia 		0.010 GeneticVariation BEFREE The polymorphism rs6855911 in SLC2A9 may be a genetic marker to assess risk of hyperuricemia among Chinese male Han population. 20972595 2011