Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs765990518
rs765990518
SLC22A12
0.800 GeneticVariation UNIPROT Hereditary Renal Hypouricemia Type 1 and Autosomal Dominant Polycystic Kidney Disease. 26418379

2015
dbSNP: rs765990518
rs765990518
SLC22A12
0.800 GeneticVariation UNIPROT Molecular analysis of the SLC22A12 (URAT1) gene in patients with primary gout. 16837472

2007
dbSNP: rs765990518
rs765990518
SLC22A12
0.800 GeneticVariation UNIPROT Mutational analysis of idiopathic renal hypouricemia in Korea. 15912381

2005
dbSNP: rs765990518
rs765990518
SLC22A12
T 0.800 GeneticVariation CLINVAR Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia. 15634722

2005
dbSNP: rs765990518
rs765990518
SLC22A12
0.800 GeneticVariation UNIPROT Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia. 15634722

2005
dbSNP: rs765990518
rs765990518
SLC22A12
0.800 GeneticVariation UNIPROT A high prevalence of renal hypouricemia caused by inactive SLC22A12 in Japanese. 15327384

2004
dbSNP: rs765990518
rs765990518
SLC22A12
T 0.800 GeneticVariation CLINVAR Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion. 14694169

2004
dbSNP: rs765990518
rs765990518
SLC22A12
0.800 GeneticVariation UNIPROT Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion. 14694169

2004
dbSNP: rs765990518
rs765990518
SLC22A12
0.800 GeneticVariation UNIPROT Molecular identification of a renal urate anion exchanger that regulates blood urate levels. 12024214

2002