Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800629
rs1800629
TNF
0.020 GeneticVariation BEFREE The TNFA rs1800629 gene polymorphism is associated with markers of kidney disease severity and distant organ dysfunction among patients with AKI. 23796916

2013

dbSNP: rs62341639
rs62341639
0.010 GeneticVariation BEFREE These include rs62341639 (metaanalysis P = 2.48 × 10<sup>-7</sup>; odds ratio [OR], 0.64; 95% confidence interval [CI], 0.55-0.76) and rs62341657 (P = 3.26 × 10<sup>-7</sup>; OR, 0.65; 95% CI, 0.55-0.76) on chromosome 4 near APOL1-regulator IRF2, and rs9617814 (metaanalysis P = 3.81 × 10<sup>-6</sup>; OR, 0.70; 95% CI, 0.60-0.81) and rs10854554 (P = 6.53 × 10<sup>-7</sup>; OR, 0.67; 95% CI, 0.57-0.79) on chromosome 22 near acute kidney injury-related gene TBX1. 27576016

2017

dbSNP: rs62341657
rs62341657
0.010 GeneticVariation BEFREE These include rs62341639 (metaanalysis P = 2.48 × 10<sup>-7</sup>; odds ratio [OR], 0.64; 95% confidence interval [CI], 0.55-0.76) and rs62341657 (P = 3.26 × 10<sup>-7</sup>; OR, 0.65; 95% CI, 0.55-0.76) on chromosome 4 near APOL1-regulator IRF2, and rs9617814 (metaanalysis P = 3.81 × 10<sup>-6</sup>; OR, 0.70; 95% CI, 0.60-0.81) and rs10854554 (P = 6.53 × 10<sup>-7</sup>; OR, 0.67; 95% CI, 0.57-0.79) on chromosome 22 near acute kidney injury-related gene TBX1. 27576016

2017

dbSNP: rs9617814
rs9617814
0.010 GeneticVariation BEFREE These include rs62341639 (metaanalysis P = 2.48 × 10<sup>-7</sup>; odds ratio [OR], 0.64; 95% confidence interval [CI], 0.55-0.76) and rs62341657 (P = 3.26 × 10<sup>-7</sup>; OR, 0.65; 95% CI, 0.55-0.76) on chromosome 4 near APOL1-regulator IRF2, and rs9617814 (metaanalysis P = 3.81 × 10<sup>-6</sup>; OR, 0.70; 95% CI, 0.60-0.81) and rs10854554 (P = 6.53 × 10<sup>-7</sup>; OR, 0.67; 95% CI, 0.57-0.79) on chromosome 22 near acute kidney injury-related gene TBX1. 27576016

2017

dbSNP: rs10854554
rs10854554
0.010 GeneticVariation BEFREE These include rs62341639 (metaanalysis P = 2.48 × 10<sup>-7</sup>; odds ratio [OR], 0.64; 95% confidence interval [CI], 0.55-0.76) and rs62341657 (P = 3.26 × 10<sup>-7</sup>; OR, 0.65; 95% CI, 0.55-0.76) on chromosome 4 near APOL1-regulator IRF2, and rs9617814 (metaanalysis P = 3.81 × 10<sup>-6</sup>; OR, 0.70; 95% CI, 0.60-0.81) and rs10854554 (P = 6.53 × 10<sup>-7</sup>; OR, 0.67; 95% CI, 0.57-0.79) on chromosome 22 near acute kidney injury-related gene TBX1. 27576016

2017

dbSNP: rs1800470
rs1800470
0.010 GeneticVariation BEFREE To investigate whether the genetic polymorphisms of rs1800470 (codon 10 T/C), rs1800471 (codon 25 C/G) from the TGF-β, and rs2430561 (+874 T/A) from IFN-γ may be a risk factor for ICU patients to the development of AKI and/or death. 25147823

2014

dbSNP: rs1800471
rs1800471
0.010 GeneticVariation BEFREE To investigate whether the genetic polymorphisms of rs1800470 (codon 10 T/C), rs1800471 (codon 25 C/G) from the TGF-β, and rs2430561 (+874 T/A) from IFN-γ may be a risk factor for ICU patients to the development of AKI and/or death. 25147823

2014

dbSNP: rs2430561
rs2430561
0.010 GeneticVariation BEFREE To investigate whether the genetic polymorphisms of rs1800470 (codon 10 T/C), rs1800471 (codon 25 C/G) from the TGF-β, and rs2430561 (+874 T/A) from IFN-γ may be a risk factor for ICU patients to the development of AKI and/or death. 25147823

2014

dbSNP: rs8094315
rs8094315
0.010 GeneticVariation BEFREE Two of these were in the BCL2 gene and both were associated with a decreased risk of acute kidney injury (rs8094315: odds ratio 0.61, p = .0002; rs12457893: odds ratio 0.67, p = .0002, both for combined data). 22710204

2012

dbSNP: rs12457893
rs12457893
0.010 GeneticVariation BEFREE Two of these were in the BCL2 gene and both were associated with a decreased risk of acute kidney injury (rs8094315: odds ratio 0.61, p = .0002; rs12457893: odds ratio 0.67, p = .0002, both for combined data). 22710204

2012

dbSNP: rs121907892
rs121907892
0.030 GeneticVariation BEFREE We here described a 25-yr-old man showing idiopathic renal hypouricemia with G774A mutation in SCL22A12 who presented exercise-induced acute renal failure. 21935282

2011

dbSNP: rs1451506414
rs1451506414
0.010 GeneticVariation BEFREE We here described a 25-yr-old man showing idiopathic renal hypouricemia with G774A mutation in SCL22A12 who presented exercise-induced acute renal failure. 21935282

2011