Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE The association was observed in HCV mono-infected (OR, 2.49; 95% CI, 1.64-3.79; P = 1.96 x 10(-5)) and HCV/HIV coinfected individuals (OR, 2.16; 95% CI, 1.47-3.18; P = 8.24 x 10(-5)). rs8099917 was also associated with failure to respond to therapy (OR, 5.19; 95% CI, 2.90-9.30; P = 3.11 x 10(-8)), with the strongest effects in patients with HCV genotype 1 or 4. 20060832

2010

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE Among 1369 Urban Health Study participants, we evaluated genetic models for the association of IL28B genotype (rs12979860 and rs8099917) with hepatitis C virus (HCV) clearance. 22013224

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE We found that the HCV genotype 1 responder genotypes at rs12979860 and rs8099917 did not associate with sustained virological response to PEG-IFN/ribavirin therapy. 21374656

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE Two single nucleotide polymorphisms were genotyped in the IL28B locus (rs12979860 and rs8099917) from 817 patients with chronic HCV infection, and substitutions at amino acids 70 and 91 of the HCV core protein and within the NS5A interferon sensitivity-determining region (ISDR) were analysed. 21068134

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE The allelic discrimination assay by Taqman real-time PCR was developed to determine genotypes of SNPs, rs12979860 and rs8099917, which were analyzed in 65 Korean patients with HCV genotype-1. 21907615

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE The purpose of the study was to establish methods for determining the SNP rs8099917 associated with IL28B, which might be useful for further research of the treatment of HCV. 21529139

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE Recent genome-wide association studies have identified two host single-nucleotide polymorphisms (SNPs) near the IL28B gene (rs12979860 C/T and rs8099917 T/G) that are associated with sustained virological response in patients infected with the hepatitis C virus. 21704279

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE The rs8099917 TT genotype is significantly independently predictive of RVR, which is the single best predictor of SVR, in Asian HCV-2 patients. 21254157

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE Common IL28B locus polymorphisms (SNPs rs8099917 and rs12979860) have been reported to affect peg-interferon plus ribavirin combination therapy (PEG-RBV) for hepatitis C virus (HCV) genotype 1b, but few reports have examined their effect on other two common genotypes, 2a and 2b. 21112660

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE Correlation analysis revealed that rs8099917 genotype was correlated with γ-glutamyl transpeptidase, hyaluronic acid, and HCV core aa 70. 21503910

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE The rs8099917 genotype and total PEG-IFN dose were associated with SVR in patients with hepatitis C virus genotype 1. 22156487

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE The aim of this study was to determine whether a single IL-28B genotype SNP rs8099917 or rs12979860 determination is sufficient to predict treatment failure in patients with chronic HCV. 21900787

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE Patients carrying both CC(rs12979860) and TT(rs8099917) genotypes achieved lower levels of HCV RNA at week 4 than those with CT or TT at rs12979860 and TT(rs8099917) (P = 0.0004). 21692944

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE IL28B SNP rs8099917 "G" was associated with absence of treatment-induced clearance (odds ratio [OR] 2.19, p = 1.27×10(-8), 1.67-2.88) and absence of spontaneous clearance (OR 3.83, p = 1.71×10(-14), 2.67-5.48) of HCV, as was rs12979860, with slightly lower ORs. 21931540

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE Among patients with HCV genotype 1b, there were differences in the reduction and subsequent increase in HCV RNA levels after administering IFN based on rs8099917 genetic polymorphisms. 21567424

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE With rs8099917, HCV genotype 1b patients had a significantly lower frequency of the favourable genotype (86.6 %) compared with healthy controls (91.7 %), and HCV genotype 2a patients had an intermediate frequency (89.9 %). 21228123

2011

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE HCV amino acid (aa) substitutions in non-structural protein 5a, including those in the IFN/RBV resistance-determining region (IRRDR) and the IFN sensitivity-determining region and the core regions, as well as the genetic variation (rs8099917) near the interleukin 28B (IL28B) gene (genotype TT) were analyzed. 22441534

2012

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE This study suggests that host genetic polymorphisms rs8099917 in the vicinity of IL-28B is the most important predictor of treatment response of PEG-IFN-α/RBV for HCV patients in China. 22713131

2012

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE The dominant HCV sequences classified by the response were subjected to systematic sliding-window comparison analysis to characterize response-specific viral sequences, along with IL28B SNP analyses (rs8099917). 22577043

2012

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE The aim of our research was to clarify study whether IL-28B gene polymorphism (rs8099917) is associated with HTLV-1/HCV co-infection. 22336134

2012

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE These results demonstrate that rs12979860, compared to rs8099917, may be a better predictor of response to the peg-IFN/RBV treatment among HCV/HIV-1 coinfected patients. 22328925

2012

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE Two single nucleotide polymorphisms (SNP, rs8099917, rs12979860) near the IL28B gene have been illustrated as outcome predictors of hepatitis C virus (HCV) treatment with pegylated interferon/ribavirin. 22257210

2012

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE Among patients with the TT genotype for rs8099917 (associated with a favorable response), the rates of sustained virologic response were higher in patients with a ≥3 log(10) reduction in serum HCV RNA levels at 4 weeks after starting therapy (P < 0.0001). 22095536

2012

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE Interleukin-28B (IL28B) single nucleotide polymorphism (SNP) influences viral response (VR) to interferon (IFN) therapy in patients with hepatitis C. We studied the relationship between VR and the IL28B polymorphism (rs8099917) in patients on long-term pegylated IFN plus ribavirin (PEGIFN/RBV) therapy for recurrent hepatitis C after living-donor liver transplantation (LDLT). 22432893

2012

dbSNP: rs8099917
rs8099917
0.100 GeneticVariation BEFREE The method constitutes a simple and reliable assay, which may be readily available for genotyping of rs12979860 and rs8099917 in laboratories that support hepatitis C treatment centers. 22664181

2012