Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 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: 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: rs72631567
rs72631567
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: 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: 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: 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: 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: 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: 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: 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: 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

dbSNP: rs5742909
rs5742909
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: rs733618
rs733618
0.010 GeneticVariation BEFREE Five haplotypes were estimated for 4 SNPs (excluding rs733618); the frequency of haplotype ACGG was significantly higher in the DILI group (68.9%) than in the non-DILI group (61.1%) (p = 0.041). 23300559

2012

dbSNP: rs80292941
rs80292941
0.010 GeneticVariation BEFREE Our findings strongly suggest that <i>LINC00152</i> may promote TB progression and highlight rs80292941 single nucleotide polymorphism as a novel predisposition marker for antituberculosis drug-induced hepatotoxicity. 29383173

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: 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: rs9274407
rs9274407
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: 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: 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: 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: 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