rs2276415
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A χ(2)-test and multivariable logistic regression analysis with adjustments for age, sex, baseline serum creatinine, and underlying comorbid disease covariates showed a significant association between rs2276415 and the prevalence of any event of acute kidney injury and chronic kidney disease (CKD) in diabetic patients but not in patients without diabetes.
|
26719361 |
2016 |
rs1370328347
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Apolipoprotein E genotype, TNF-α 308G/A and risk for cardiac surgery associated-acute kidney injury in Caucasians.
|
24059882 |
2014 |
rs767816037
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Apolipoprotein E genotype, TNF-α 308G/A and risk for cardiac surgery associated-acute kidney injury in Caucasians.
|
24059882 |
2014 |
rs1444669684
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Both tumors develop in mice upon conditional deletion in melanocytes of Ink4a/Arf tumor suppressor genes with concomitant expression of oncogene H-Ras(G12V) and a known tumor antigen.
|
23173060 |
2012 |
rs4680
|
|
|
0.030 |
GeneticVariation |
BEFREE |
COMT-Val158Met-polymorphism is not a risk factor for acute kidney injury after cardiac surgery.
|
24167357 |
2013 |
rs775020499
|
|
|
0.010 |
GeneticVariation |
BEFREE |
COMT-Val158Met-polymorphism is not a risk factor for acute kidney injury after cardiac surgery.
|
24167357 |
2013 |
rs1800629
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Despite the numerous, although contradictory, studies about association between polymorphisms rs1800629 in <i>TNFA</i> and rs1800896 in <i>IL10</i> and AKI, we found no association (odds ratios 1.06 (95% CI 0.89⁻1.28, <i>p</i> = 0.51) and 0.92 (95% CI 0.80⁻1.05, <i>p</i> = 0.20), respectively).
|
30862128 |
2019 |
rs1800896
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Despite the numerous, although contradictory, studies about association between polymorphisms rs1800629 in <i>TNFA</i> and rs1800896 in <i>IL10</i> and AKI, we found no association (odds ratios 1.06 (95% CI 0.89⁻1.28, <i>p</i> = 0.51) and 0.92 (95% CI 0.80⁻1.05, <i>p</i> = 0.20), respectively).
|
30862128 |
2019 |
rs1050851
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In Caucasian patients, we identified associations between two SNPs and the incidence of AKI (stage 1 and above): rs1050851 and rs2233417; both are found within the gene for nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha (NFKBIA).
|
26477820 |
2015 |
rs2233417
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In Caucasian patients, we identified associations between two SNPs and the incidence of AKI (stage 1 and above): rs1050851 and rs2233417; both are found within the gene for nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha (NFKBIA).
|
26477820 |
2015 |
rs2233406
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In conclusion, <i>NFKB1</i> rs28362491, <i>NFKBIA</i> rs2233406 and <i>NFKBIA</i> rs696 polymorphisms may serve as biomarkers for predicting risk of AKI in children.
|
30429237 |
2018 |
rs696
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In conclusion, <i>NFKB1</i> rs28362491, <i>NFKBIA</i> rs2233406 and <i>NFKBIA</i> rs696 polymorphisms may serve as biomarkers for predicting risk of AKI in children.
|
30429237 |
2018 |
rs1800777
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the Derivation Cohort, one genetic variant in the Cholesteryl Ester Transfer Protein (CETP) gene, rs1800777 (allele A), was strongly associated with lower HDL-C levels (17.4 mg/dL vs. 32.9 mg/dL, P = 0.002), greater CETP mass (3.43 µg/mL vs. 1.32 µg/mL, P = 0.034), and increased risk of clinically significant sepsis-associated AKI (OR: 8.28, p = 0.013).
|
30425299 |
2018 |
rs782818582
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Novel compound heterozygote mutations (H234Q/R1206X) of the ADAMTS13 gene in an adult patient with Upshaw-Schulman syndrome showing predominant episodes of repeated acute renal failure.
|
16449289 |
2006 |
rs561633150
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our findings suggest that homozygous and/or compound heterozygous loss-of-function mutations p.G216R and p.N333S cause renal hypouricaemia via loss of uric acid absorption and do lead to acute kidney injury.
|
22527535 |
2012 |
rs753482595
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Our findings suggest that homozygous and/or compound heterozygous loss-of-function mutations p.G216R and p.N333S cause renal hypouricaemia via loss of uric acid absorption and do lead to acute kidney injury.
|
22527535 |
2012 |
rs1799983
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Patients with the TT-homozygous genotype of eNOS G894T had more severe PUUV-induced AKI than the other genotypes.
|
26561052 |
2015 |
rs4680
|
|
|
0.030 |
GeneticVariation |
BEFREE |
Pilot study of association of catechol-O-methyl transferase rs4680 genotypes with acute kidney injury and tubular stress after open heart surgery.
|
25525983 |
2014 |
rs121907892
|
|
|
0.030 |
GeneticVariation |
BEFREE |
She had compound heterozygous mutations in this gene (W258X and IVS2+1G>A), nevertheless, she showed no clinical manifestations such as urolithiasis and exercise-induced acute renal failure.
|
16724660 |
2006 |
rs4680
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The aim of the current study is to prospectively investigate the impact of the COMT rs4680 polymorphism on the incidence of AKI in patients undergoing cardiac surgery.
|
29426301 |
2018 |
rs41507953
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The EPHX2 Lys55Arg polymorphism is associated with AKI following cardiac surgery in patients without preexisting CKD.
|
28552948 |
2017 |
rs121907896
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The patient had compound heterozygous mutations in the hURAT1 gene (R90H and W258X), but showed no clinical manifestations such as urolithiasis or exercise-induced acute renal failure.
|
17362586 |
2007 |
rs121907892
|
|
|
0.030 |
GeneticVariation |
BEFREE |
The patient had compound heterozygous mutations in the hURAT1 gene (R90H and W258X), but showed no clinical manifestations such as urolithiasis or exercise-induced acute renal failure.
|
17362586 |
2007 |
rs2093266
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The SNPs rs2093266 in the SERPINA4 and rs1955656 in the SERPINA5 were associated with the development of severe AKI (KDIGO stage 2-3) in critically ill patients with septic shock.
|
28270177 |
2017 |
rs1955656
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The SNPs rs2093266 in the SERPINA4 and rs1955656 in the SERPINA5 were associated with the development of severe AKI (KDIGO stage 2-3) in critically ill patients with septic shock.
|
28270177 |
2017 |