SLC2A9, solute carrier family 2 member 9, 56606

N. diseases: 74; N. variants: 389
Disease: Uric acid measurement (procedure) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs56223908
rs56223908
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		C 0.700 GeneticVariation GWASCAT Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps. 27668658 2016