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: rs13111638
rs13111638
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.800 GeneticVariation GWASDB A genome-wide association study of serum uric acid in African Americans. 21294900 2011
dbSNP: rs3775948
rs3775948
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		G 0.800 GeneticVariation GWASDB A genome-wide association study of serum uric acid in African Americans. 21294900 2011
dbSNP: rs3775948
rs3775948
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		G 0.800 GeneticVariation GWASCAT A genome-wide association study of serum uric acid in African Americans. 21294900 2011
dbSNP: rs6449213
rs6449213
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.800 GeneticVariation GWASDB A genome-wide association study of serum uric acid in African Americans. 21294900 2011
dbSNP: rs10939650
rs10939650
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASDB A genome-wide association study of serum uric acid in African Americans. 21294900 2011
dbSNP: rs13113918
rs13113918
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASDB A genome-wide association study of serum uric acid in African Americans. 21294900 2011
dbSNP: rs3733588
rs3733588
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASDB A genome-wide association study of serum uric acid in African Americans. 21294900 2011
dbSNP: rs4529048
rs4529048
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASDB A genome-wide association study of serum uric acid in African Americans. 21294900 2011
dbSNP: rs7663032
rs7663032
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASDB A genome-wide association study of serum uric acid in African Americans. 21294900 2011
dbSNP: rs16890979
rs16890979
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		T 0.800 GeneticVariation GWASCAT Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. 18834626 2008
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
dbSNP: rs6449213
rs6449213
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		T 0.800 GeneticVariation GWASCAT Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. 28270201 2017
dbSNP: rs16890979
rs16890979
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.800 GeneticVariation GWASDB Followup genotyping revealed that a nonsynonymous coding SNP (Val253Ile; rs16890979) in GLUT9 was most strongly associated with uric acid levels, with each copy of the minor allele associated with a decrease of 0.47 mg/dl in the uric acid level (95% confidence interval 0.31-0.63 [P = 1.43 x 10(-11)]). 18759275 2008
dbSNP: rs16890979
rs16890979
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.800 GeneticVariation GWASCAT Followup genotyping revealed that a nonsynonymous coding SNP (Val253Ile; rs16890979) in GLUT9 was most strongly associated with uric acid levels, with each copy of the minor allele associated with a decrease of 0.47 mg/dl in the uric acid level (95% confidence interval 0.31-0.63 [P = 1.43 x 10(-11)]). 18759275 2008
dbSNP: rs4385059
rs4385059
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.800 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs34325511
rs34325511
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs61112052
rs61112052
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs73221597
rs73221597
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs76099163
rs76099163
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs7679724
rs7679724
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs7675964
rs7675964
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.800 GeneticVariation GWASCAT Genetic contributors to serum uric acid levels in Mexicans and their effect on premature coronary artery disease. 30305239 2019
dbSNP: rs7678287
rs7678287
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		A 0.700 GeneticVariation GWASCAT Genetic contributors to serum uric acid levels in Mexicans and their effect on premature coronary artery disease. 30305239 2019
dbSNP: rs7671266
rs7671266
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		T 0.800 GeneticVariation GWASCAT Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. 21943158 2011
dbSNP: rs13111638
rs13111638
Entrez Id: 56606;105374476
Gene Symbol: SLC2A9;LOC105374476
SLC2A9;LOC105374476
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		T 0.800 GeneticVariation GWASCAT Genetics of serum urate concentrations and gout in a high-risk population, patients with chronic kidney disease. 30181573 2018
dbSNP: rs16890979
rs16890979
Entrez Id: 56606
Gene Symbol: SLC2A9
SLC2A9
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		A 0.800 GeneticVariation GWASCAT Genome wide association study of uric acid in Indian population and interaction of identified variants with Type 2 diabetes. 26902266 2016