SLC17A1, solute carrier family 17 member 1, 6568

N. diseases: 23; N. variants: 164
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: rs1165196
rs1165196
Entrez Id: 6568
Gene Symbol: SLC17A1
SLC17A1
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: rs1165196
rs1165196
Entrez Id: 6568
Gene Symbol: SLC17A1
SLC17A1
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		G 0.800 GeneticVariation GWASCAT Modulation of genetic associations with serum urate levels by body-mass-index in humans. 25811787 2015
dbSNP: rs1165196
rs1165196
Entrez Id: 6568
Gene Symbol: SLC17A1
SLC17A1
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		G 0.800 GeneticVariation GWASCAT Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. 20884846 2010
dbSNP: rs1165196
rs1165196
Entrez Id: 6568
Gene Symbol: SLC17A1
SLC17A1
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		0.800 GeneticVariation GWASDB Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. 19503597 2009