|
rs99780
|
|
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 |
|
rs995922697
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We prospectively enrolled multicenter patients with end-stage renal disease (ESRD) and those without chronic kidney disease (CKD) of Han Chinese origin, with SOD2 (Val16Ala), GPX1 (Pro197Leu), and PPAR-γ (Pro12Ala, C161T) genotyped.
|
26881045 |
2016 |
|
rs9895661
|
|
C |
0.700 |
GeneticVariation |
GWASCAT |
New loci associated with kidney function and chronic kidney disease.
|
20383146 |
2010 |
|
rs9895661
|
|
C |
0.700 |
GeneticVariation |
GWASCAT |
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
|
31152163 |
2019 |
|
rs9830664
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population.
|
29124443 |
2018 |
|
rs9749262
|
|
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 |
|
rs97384
|
|
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 |
|
rs968567
|
|
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 |
|
rs963837
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
|
26831199 |
2016 |
|
rs963837
|
|
T |
0.700 |
GeneticVariation |
GWASCAT |
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
|
31152163 |
2019 |
|
rs9395890
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our findings indicate that rs9395890 is associated with susceptibility to ESRD in Taiwan population.
|
31382928 |
2019 |
|
rs9379832
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genetics of serum urate concentrations and gout in a high-risk population, patients with chronic kidney disease.
|
30181573 |
2018 |
|
rs9379084
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A meta-analysis combining African American and European American T2D-ESKD data revealed P = 3.52 × 10(-7) and 3.70 × 10(-5) for rs9379084 and rs41302867 association, respectfully.
|
25027322 |
2014 |
|
rs9374
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The other three SNPs (rs10951982, rs6954996, and rs9374), in all comparison models, were not associated with ESRD risk (P > 0.05).
|
26841219 |
2016 |
|
rs9369717
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However, when genotype frequencies in patients with ESRD were compared with all other patients, two CD2AP SNPs, rs9369717 and rs9349417, were found to be associated with ESRD.
|
23681557 |
2013 |
|
rs9349417
|
|
|
0.010 |
GeneticVariation |
BEFREE |
However, when genotype frequencies in patients with ESRD were compared with all other patients, two CD2AP SNPs, rs9369717 and rs9349417, were found to be associated with ESRD.
|
23681557 |
2013 |
|
rs9298190
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We observed the strongest evidence for association between ESRD and rs1749824, located in the ZMIZ1 gene [OR = 1.47 (1.21-1.78) per copy of T allele; P = 8.1 x 10(-5)] and rs9298190, located in the musculin gene [OR = 1.56 (1.28-1.91) per copy of C allele; P = 1.6 x 10(-5)].
|
19929986 |
2009 |
|
rs926632
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The minor allele of rs260741, rs197173, and rs926632 in EDN3 were associated with reduced risk of hospitalized bacteremia events in ESRD patients.
|
31167651 |
2019 |
|
rs926392
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association scan for survival on dialysis in African-Americans with type 2 diabetes.
|
21546767 |
2011 |
|
rs911119
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
New loci associated with kidney function and chronic kidney disease.
|
20383146 |
2010 |
|
rs904520404
|
|
|
0.010 |
GeneticVariation |
BEFREE |
This condition is a renal-hepatic ciliopathy with phenotypic characteristics that include hepatosplenomegaly, hepatic fibrosis with bile cholestasis, increased kidney echogenicity, and end-stage renal disease.Here, we report a 13-year-old African-Caribbean female with areas of absence of heterozygosity suggesting parental consanguinity or identity by decent due to the founder effect, harboring a novel homozygous pathogenic variant (c.383C>G, p.S128*) in exon 3 of DCDC2.
|
31821705 |
2020 |
|
rs890336
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The risk haplotypes (rs6566810, rs17089362 [A,T] and rs6566810, rs17089362, rs890336 [A,T,C]) were most strongly associated with DM-ESRD among African-Americans in the non 5L-5L group.
|
19373489 |
2009 |
|
rs881858
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
New loci associated with kidney function and chronic kidney disease.
|
20383146 |
2010 |
|
rs868822
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
|
31152163 |
2019 |
|
rs867394500
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We studied retrospectively the role of angiotensinogen (AGT) M235T, angiotensin converting enzyme (ACE) insertion/deletion (I/D), angiotensin II type 1 receptor (AT1R) A1166C, aldosterone syntase (CYP11B2) -344C/T and intron 2 W/C polymorphisms in conjunction with clinical and biochemical covariables on the rate of progression of renal insufficiency in a group of patients with ESRD of various etiologies.
|
12832734 |
2003 |