Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13333226
rs13333226
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
A 0.810 GeneticVariation GWASCAT Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. 27618447

2016

dbSNP: rs13333226
rs13333226
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
A 0.810 GeneticVariation GWASCAT In a subset of 13,446 individuals with estimated glomerular filtration rate (eGFR) measurements, we show that rs13333226 is independently associated with hypertension (unadjusted for eGFR: 0.89 [0.83-0.96], p = 0.004; after eGFR adjustment: 0.89 [0.83-0.96], p = 0.003). 21082022

2010

dbSNP: rs12917707
rs12917707
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
T 0.800 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199

2016

dbSNP: rs4293393
rs4293393
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
T 0.800 GeneticVariation GWASCAT Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. 20686651

2010

dbSNP: rs12917707
rs12917707
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
T 0.720 GeneticVariation GWASCAT Genome-wide association study of kidney function decline in individuals of European descent. 25493955

2015

dbSNP: rs12917707
rs12917707
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
T 0.720 GeneticVariation GWASCAT New loci associated with kidney function and chronic kidney disease. 20383146

2010

dbSNP: rs12917707
rs12917707
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
G 0.720 GeneticVariation GWASCAT Multiple loci associated with indices of renal function and chronic kidney disease. 19430482

2009

dbSNP: rs13333226
rs13333226
CUI: C0011847
Disease: Diabetes
Diabetes
0.710 GeneticVariation GWASCAT A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. 29703844

2018

dbSNP: rs13333226
rs13333226
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.710 GeneticVariation GWASCAT A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. 29703844

2018

dbSNP: rs12917707
rs12917707
CUI: C0011847
Disease: Diabetes
Diabetes
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199

2016

dbSNP: rs12917707
rs12917707
Creatinine measurement, serum (procedure)
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199

2016

dbSNP: rs12917707
rs12917707
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199

2016

dbSNP: rs12917707
rs12917707
Creatinine measurement, serum (procedure)
T 0.700 GeneticVariation GWASCAT New loci associated with kidney function and chronic kidney disease. 20383146

2010

dbSNP: rs12922822
rs12922822
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019

dbSNP: rs12922822
rs12922822
CUI: C0011847
Disease: Diabetes
Diabetes
T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019

dbSNP: rs12922822
rs12922822
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708

2019

dbSNP: rs12922822
rs12922822
CUI: C4280669
Disease: Velopharyngeal dysfunction
Velopharyngeal dysfunction
0.700 GeneticVariation GWASCAT GWAS reveals loci associated with velopharyngeal dysfunction. 29855589

2018

dbSNP: rs13329952
rs13329952
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
T 0.700 GeneticVariation GWASCAT Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies. 30604766

2019

dbSNP: rs13329952
rs13329952
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199

2016

dbSNP: rs13329952
rs13329952
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199

2016

dbSNP: rs13329952
rs13329952
Creatinine measurement, serum (procedure)
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199

2016

dbSNP: rs13333226
rs13333226
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 GeneticVariation GWASCAT A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. 29703844

2018

dbSNP: rs13333226
rs13333226
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation GWASCAT A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. 29703844

2018

dbSNP: rs13333226
rs13333226
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
A 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878

2017

dbSNP: rs143583842
rs143583842
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia
0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443

2018