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: rs2762353
rs2762353
Entrez Id: 6568
Gene Symbol: SLC17A1
SLC17A1
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		A 0.800 GeneticVariation GWASCAT Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. 31578528 2019
dbSNP: rs2762353
rs2762353
Entrez Id: 6568
Gene Symbol: SLC17A1
SLC17A1
CUI: C0202239
Disease:
Uric acid measurement (procedure) 		A 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals. 30993211 2019
dbSNP: rs2762353
rs2762353
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