Gene: UMOD ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4293393
rs4293393
UMOD
T 0.800 GeneticVariation GWASDB Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. 20686651

2010
dbSNP: rs4293393
rs4293393
UMOD
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
UMOD
T 0.720 GeneticVariation GWASCAT Genome-wide association study of kidney function decline in individuals of European descent. 25493955

2015
dbSNP: rs12917707
rs12917707
UMOD
0.720 GeneticVariation BEFREE We tested a large cohort of Caucasian patients for association of rs12917707 with IgA nephropathy showing a benign, stable course and with IgA nephropathy that progressed toward end stage renal failure. 25163389

2014
dbSNP: rs12917707
rs12917707
UMOD
0.720 GeneticVariation BEFREE The rs12917707 minor allele showed association with lower risk of ESRD (OR 0.89 [0.76-1.03], p = 0.04) consistent in effect size and direction with the previous report (Böger et al, PLoS Genet 2011). 22947327

2012
dbSNP: rs12917707
rs12917707
UMOD
T 0.720 GeneticVariation GWASCAT New loci associated with kidney function and chronic kidney disease. 20383146

2010
dbSNP: rs12917707
rs12917707
UMOD
G 0.720 GeneticVariation GWASCAT Multiple loci associated with indices of renal function and chronic kidney disease. 19430482

2009
dbSNP: rs201761378
rs201761378
UMOD
0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443

2018
dbSNP: rs13329952
rs13329952
UMOD
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199

2016
dbSNP: rs183962941
rs183962941
UMOD
0.010 GeneticVariation BEFREE One SNP (rs183962941), located in a non-coding region of UMOD, was nominally associated with ESRD (p = 0.008). 28609449

2017
dbSNP: rs13333226
rs13333226
UMOD
0.010 GeneticVariation BEFREE A common variation rs13333226 in the promoter region of UMOD gene was independently associated with ESRD in Han Chinese. 27938332

2016