Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1047891
rs1047891
CPS1
A 0.800 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs12460876
rs12460876
SLC7A9
C 0.800 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs1047891
rs1047891
CPS1
0.800 GeneticVariation GWASDB Genome-wide association and functional follow-up reveals new loci for kidney function. 22479191

2012
dbSNP: rs12460876
rs12460876
SLC7A9
0.800 GeneticVariation GWASDB Genome-wide association and functional follow-up reveals new loci for kidney function. 22479191

2012
dbSNP: rs1047891
rs1047891
CPS1
A 0.800 GeneticVariation GWASDB New loci associated with kidney function and chronic kidney disease. 20383146

2010
dbSNP: rs12460876
rs12460876
SLC7A9
C 0.800 GeneticVariation GWASDB New loci associated with kidney function and chronic kidney disease. 20383146

2010
dbSNP: rs12917707
rs12917707
UMOD
0.730 GeneticVariation BEFREE The genetic rs12917707-G>T variant in uromodulin (UMOD) has been associated with renal function, chronic kidney disease and hypertension with the minor T-allele showing a protective effect. 28418009

2018
dbSNP: rs12917707
rs12917707
UMOD
0.730 GeneticVariation BEFREE The rs12917707 was not associated with CKD. 28954491

2017
dbSNP: rs12917707
rs12917707
UMOD
0.730 GeneticVariation BEFREE In recent genetic association studies, common variants including rs12917707 in the UMOD locus have shown strong evidence of association with eGFR, prevalent and incident chronic kidney disease and uromodulin urinary concentration in general population cohorts. 22947327

2012
dbSNP: rs12917707
rs12917707
UMOD
0.730 GeneticVariation GWASDB Genome-wide association and functional follow-up reveals new loci for kidney function. 22479191

2012
dbSNP: rs12917707
rs12917707
UMOD
T 0.730 GeneticVariation GWASDB New loci associated with kidney function and chronic kidney disease. 20383146

2010
dbSNP: rs7805747
rs7805747
PRKAG2
0.710 GeneticVariation BEFREE Using GWAS analysis in PhenoScanner, we showed that rs7805747 is not only associated with CKD, but also is significantly associated with other diseases or phenotypes. 30559760

2018
dbSNP: rs1260326
rs1260326
GCKR
0.710 GeneticVariation BEFREE The present study suggests a possible association of the T/T genotype of GCKR rs1260326 polymorphism with elevated risk of CKD and its interaction with current smoking, which may support the possibility of performing risk evaluation and prevention of this potentially life-threatening disease based on genetic traits in the near future. 24535998

2014
dbSNP: rs1260326
rs1260326
GCKR
0.710 GeneticVariation GWASDB Genome-wide association and functional follow-up reveals new loci for kidney function. 22479191

2012
dbSNP: rs7805747
rs7805747
PRKAG2
0.710 GeneticVariation GWASDB Genome-wide association and functional follow-up reveals new loci for kidney function. 22479191

2012
dbSNP: rs1260326
rs1260326
GCKR
T 0.710 GeneticVariation GWASDB New loci associated with kidney function and chronic kidney disease. 20383146

2010
dbSNP: rs7805747
rs7805747
PRKAG2
A 0.710 GeneticVariation GWASDB New loci associated with kidney function and chronic kidney disease. 20383146

2010
dbSNP: rs10178409
rs10178409 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs1020120
rs1020120
LOC102724036
T 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs102274
rs102274
TMEM258
C 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs102275
rs102275
TMEM258
C 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs1066621
rs1066621 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs1077989
rs1077989
GPHN ; TMEM229B
C 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs112201728
rs112201728
SLC22A1
T 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
dbSNP: rs112329286
rs112329286
SYNE2
TTTTA 0.700 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018