Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1041983
rs1041983
0.010 GeneticVariation BEFREE Two SNPs in NAT2 (rs1041983 and rs1495741) and NAT2 slow acetylators (SA) were significantly associated with INH-DILI (OR (95% CI) = 13.86 (4.30-44.70), 0.10 (0.03-0.33) and 9.98 (3.32-33.80), respectively). 29036176

2017

dbSNP: rs1050450
rs1050450
0.010 GeneticVariation BEFREE We have evaluated possible associations between the risk of developing DILI and common genetic variants of the manganese superoxide dismutase (SOD2 Val16Ala) and glutathione peroxidase (GPX1 Pro200Leu) genes, which are involved in mitochondrial oxidative stress management. 20578157

2010

dbSNP: rs10946737
rs10946737
0.010 GeneticVariation BEFREE On the basis of this case-control study, SNP rs10946737 in FAM65B may be associated with susceptibility to ATDH in Chinese Han anti-TB treatment patients. 30720667

2019

dbSNP: rs114577328
rs114577328
0.010 GeneticVariation BEFREE We associated DILI with rs114577328 (a proxy for A*33:01 a HLA class I allele; odds ratio [OR], 2.7; 95% confidence interval [CI], 1.9-3.8; P = 2.4 × 10<sup>-8</sup>) and with rs72631567 on chromosome 2 (OR, 2.0; 95% CI, 1.6-2.5; P = 9.7 × 10<sup>-9</sup>). 28043905

2017

dbSNP: rs116561224
rs116561224
0.010 GeneticVariation BEFREE We did not associate any specific drug classes with genetic polymorphisms, except for statin-associated DILI, which was associated with rs116561224 on chromosome 18 (OR, 5.4; 95% CI, 3.0-9.5; P = 7.1 × 10<sup>-9</sup>). 28043905

2017

dbSNP: rs117806152
rs117806152
0.010 GeneticVariation BEFREE Rs79280755 increased the risk of ATDILI significantly whether in additive (OR = 3.218, 95% CI: 1.686-6.139, PBonferroni correction = .003) or dominant model (PBonferroni correction = .003), as well as rs117806152 (Additive model: PBonferroni correction = .05; dominant model: PBonferroni correction = .03). 31689868

2019

dbSNP: rs1214110864
rs1214110864
0.010 GeneticVariation BEFREE Four highly conserved nonsynonymous mutations were specific for drug-induced liver injury [ABCB11: D676Y (drug-induced cholestasis) and G855R (drug-induced cholestasis); ABCB4: I764L (drug-induced cholestasis) and L1082Q (drug-induced hepatocellular injury)]. 17264802

2007

dbSNP: rs138642043
rs138642043
0.010 GeneticVariation BEFREE On sequencing, ATP8B1 was normal in both patients although the younger was heterozygous for the c.2093G>A mutation in ABCB11, a polymorphism previously encountered in drug-induced liver injury. 23750872

2013

dbSNP: rs1495741
rs1495741
0.030 GeneticVariation BEFREE tagSNP rs1495741 as a useful molecular marker to predict antituberculosis drug-induced hepatotoxicity. 27104815

2016

dbSNP: rs1495741
rs1495741
0.030 GeneticVariation BEFREE The NAT2 tag SNP rs1495741 correlates with the susceptibility of antituberculosis drug-induced hepatotoxicity. 23407048

2013

dbSNP: rs1495741
rs1495741
0.030 GeneticVariation BEFREE Two SNPs in NAT2 (rs1041983 and rs1495741) and NAT2 slow acetylators (SA) were significantly associated with INH-DILI (OR (95% CI) = 13.86 (4.30-44.70), 0.10 (0.03-0.33) and 9.98 (3.32-33.80), respectively). 29036176

2017

dbSNP: rs17036170
rs17036170
0.700 GeneticVariation GWASDB Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs. 22968431

2012

dbSNP: rs1800796
rs1800796
0.010 GeneticVariation BEFREE rs1800796 of the IL6 gene is associated with increased risk for anti-tuberculosis drug-induced hepatotoxicity in Chinese Han children. 30029918

2018

dbSNP: rs1966862
rs1966862
0.010 GeneticVariation BEFREE This study suggested rs1966862 (ARHGAP24) and the other SNPs to be predictive factors for drug-induced hepatotoxicity during the maintenance phase in pediatric patients with ALL or LBL. 20670164

2010

dbSNP: rs2287622
rs2287622
0.020 GeneticVariation BEFREE A common variant (rs2287622; p.V444A) in the gene encoding BSEP has been associated with an increased risk of cholestatic DILI. 30608704

2019

dbSNP: rs2287622
rs2287622
0.020 GeneticVariation BEFREE Patients carrying the C allele in the ABCB11 1331T>C polymorphism are at increased risk of developing hepatocellular type of DILI, when taking drugs containing a carbocyclic system with aromatic rings. 23701583

2013

dbSNP: rs2306283
rs2306283
0.010 GeneticVariation BEFREE We found that rs12422149 of SLCO2B1, rs2032582_AT of ABCB1, rs2306283 of SLCO1B1 and rs4148323 of UGT1A1 exhibited a significant association with MMI-DILI; however, no significant difference existed after Bonferroni correction. 31240859

2019

dbSNP: rs231775
rs231775
0.010 GeneticVariation BEFREE A significant association was found between the rs231775 genotype and an early onset of DILI in the recipients. 23300559

2012

dbSNP: rs2476601
rs2476601
0.010 GeneticVariation BEFREE We associated idiosyncratic DILI with rs2476601, a nonsynonymous polymorphism that encodes a substitution of tryptophan with arginine in the protein tyrosine phosphatase, nonreceptor type 22 gene (PTPN22) (odds ratio [OR] 1.44; 95% confidence interval [CI] 1.28-1.62; P = 1.2 × 10<sup>-9</sup> and replicated the finding in the validation set (OR 1.48; 95% CI 1.09-1.99; P = .01). 30664875

2019

dbSNP: rs2741045
rs2741045
0.010 GeneticVariation BEFREE We observed statistically significant associations between SNP rs2741045 and DILI at</span> both allele and genotype levels (allele: P=0.032; genotype: P=0.029; after Bonferroni correction). 25446781

2015

dbSNP: rs3087243
rs3087243
0.010 GeneticVariation BEFREE We investigated the association of 5 CTLA4 single-nucleotide polymorphisms (SNPs) (rs733618 C/T, rs4553808 A/G, rs5742909 C/T, rs231775 A/G, and rs3087243 G/A) with drug-induced liver injury (DILI) in Chinese renal transplantation (RT) recipients. 23300559

2012

dbSNP: rs3135388
rs3135388
0.010 GeneticVariation BEFREE The strongest effect was with an HLA class II SNP (rs9274407, P=4.8×10(-14)), which correlated with rs3135388, a tag SNP of HLA-DRB1*1501-DQB1*0602 that was previously associated with AC-DILI. 21570397

2011

dbSNP: rs4148323
rs4148323
0.010 GeneticVariation BEFREE We found that rs12422149 of SLCO2B1, rs2032582_AT of ABCB1, rs2306283 of SLCO1B1 and rs4148323 of UGT1A1 exhibited a significant association with MMI-DILI; however, no significant difference existed after Bonferroni correction. 31240859

2019

dbSNP: rs4430924
rs4430924
0.010 GeneticVariation BEFREE After correcting for weight and hepatoprotectant use, conditional logistic regression analysis showed that patients carrying the AA genotype of rs4430924 in</span> XPO1 were at higher risk of anti-TB drug-induced hepatotoxicity than those carrying the GG genotype based on the subgroup of probable cases (adjusted OR, 1.938; 95%CI, 1.035-3.628; P = .039), and marginally significant differences were also found under the recessive model (P = .048) and the additive model (P = .047). 30817003

2019

dbSNP: rs4553808
rs4553808
0.010 GeneticVariation BEFREE We investigated the association of 5 CTLA4 single-nucleotide polymorphisms (SNPs) (rs733618 C/T, rs4553808 A/G, rs5742909 C/T, rs231775 A/G, and rs3087243 G/A) with drug-induced liver injury (DILI) in Chinese renal transplantation (RT) recipients. 23300559

2012