Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11881222
rs11881222
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.060 GeneticVariation BEFREE Multivariate logistic regression of the three markers showed that the A/A genotypes in both rs11506105 (EFGR) and rs11881222 (IL28B), and the C/C genotype in rs12979860 (IL28B) are associated with HCV clearance (recessive model: odds ratio (OR)=2.06, 95% confidence interval (95% CI)=1.09-3.88, P=0.025; OR=2.09, 95% CI=1.23-3.60, P=0.007; and OR=1.95, 95% CI=1.15-3.35, P=0.014 for rs11506105, rs12979860 and rs11881222, respectively). 26378651

2015

dbSNP: rs11881222
rs11881222
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.060 GeneticVariation BEFREE This study demonstrated that Indonesian patients with chronic hepatitis C (mostly ethnic Java people) mostly were infected with hepatitis C virus (HCV) genotype 1; however, they carried mainly the major genotypes of interleukin 28B (IL-28B) single nucleotide polymorphisms (SNPs) (rs12979860 CC, rs11881222 TT, rs8103142 AA, and rs8099917 TT), and they mostly achieved sustained virological responses to pegylated interferon/ribavirin treatment. 24696021

2014

dbSNP: rs11881222
rs11881222
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.060 GeneticVariation BEFREE Haplotype analysis showed that IL28B (rs12980275, rs11881222, rs12979860 and rs8099917) haplotype AACT had a protective effect for HCV infection (OR = 0.52, 95% CI = 0.33-0.83, P = 0.00551). 24144988

2014

dbSNP: rs11881222
rs11881222
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.060 GeneticVariation BEFREE To estimate the impact of interleukin 28B (IL28B) polymorphisms (rs12980275, rs8099917, rs7248668, and rs11881222) and their haplotypes on hepatitis C virus (HCV) treatment (peg-interferon-α and ribavirin) success in 324 HIV/HCV-coinfected patients. 23135173

2013

dbSNP: rs11881222
rs11881222
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.060 GeneticVariation BEFREE The major alleles of IL28B (rs12980275 A, rs11881222 A, rs8099917 T, and rs7248668 G) are associated with increased odds of liver disease severity in HIV patients infected with HCV-genotype 3. 23103287

2013

dbSNP: rs11881222
rs11881222
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.060 GeneticVariation BEFREE The exonic rs8103142 CT, the promoter rs12979860 CT and the intronic rs11881222 AG genotypes were associated with a decreased HCV clearance rate with adjusted odds ratios (aOR) of 0.3 (95% CI, 0.1-0.7), 0.4 (95% CI, 0.2-0.8) and 0.4 (95% CI, 0.2-0.8), respectively. 21070502

2011

dbSNP: rs8103142
rs8103142
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.050 GeneticVariation BEFREE We tested the association of spontaneous clearance and three single nucleotide polymorphisms (SNPs) near the Interferon-lambda 3 (IFNL3) gene (rs12979860, rs8099917, functional variant rs8103142) and compared the SNP frequencies between HIV-HCV co-infected whites and Aboriginals from the Canadian Co-infection Cohort. 25803108

2015

dbSNP: rs8103142
rs8103142
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.050 GeneticVariation BEFREE This study demonstrated that Indonesian patients with chronic hepatitis C (mostly ethnic Java people) mostly were infected with hepatitis C virus (HCV) genotype 1; however, they carried mainly the major genotypes of interleukin 28B (IL-28B) single nucleotide polymorphisms (SNPs) (rs12979860 CC, rs11881222 TT, rs8103142 AA, and rs8099917 TT), and they mostly achieved sustained virological responses to pegylated interferon/ribavirin treatment. 24696021

2014

dbSNP: rs8103142
rs8103142
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.050 GeneticVariation BEFREE Our aim was to establish an association between three IL28B SNPs (rs8099917, rs12979860, and rs8103142) and the peg-IFNα/RBV treatment response in a Mexican population cohort with chronic HCV. 23109451

2013

dbSNP: rs8103142
rs8103142
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.050 GeneticVariation BEFREE We examined whether the combined determination of the IL28B single-nucleotide polymorphisms (SNPs), rs12979860, rs8099917, rs12980275, and rs8103142, might improve the prediction of SVR in patients with HCV. 22234924

2012

dbSNP: rs8103142
rs8103142
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.050 GeneticVariation BEFREE Further, we found significant differences in HCV RNA levels among individuals chronically infected with HCV genotype 1 for rs8103142 and rs12979860 (P ≤ 0.05). 21070502

2011

dbSNP: rs4803217
rs4803217
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.040 GeneticVariation BEFREE The rs4803217 SNP is a strong, independent and superior predictor of SVR and relapse in HCV genotype 1 infected CHC patients treated with PEG-IFN-α and RBV. 28638221

2017

dbSNP: rs4803217
rs4803217
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.040 GeneticVariation BEFREE Among AA participants, associations were stronger for IFNL4-ΔG/TT than rs4803217 for undetectable HCV RNA at week 24 in Virahep-C (p=0.03) and week 20 in HALT-C (p=0.03), as well as for spontaneous HCV clearance (p=0.048). 26186989

2015

dbSNP: rs4803217
rs4803217
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.040 GeneticVariation BEFREE We analyzed a variant (rs4803217 G/T) located within the IFNL3 mRNA 3' untranslated region (UTR); the G allele (protective allele) is associated with elevated therapeutic HCV clearance. 26531896

2015

dbSNP: rs4803217
rs4803217
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.040 GeneticVariation BEFREE This analysis included the two strongest tag predictors for HCV clearance, rs8099917 and rs12979860, and four causal variants (rs4803219, rs28416813, rs8103142, and rs4803217) located in the IL28B promoter, coding, and 3'-untranslated regions. 22328925

2012

dbSNP: rs142346548
rs142346548
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.030 GeneticVariation BEFREE Significant modulation of IFN-λ4 activity by a genetic variant (P70S) supports IFN-λ4, and not other type III IFNs encoded in the same genomic locus, as the primary functional cause of the association with HCV clearance. 31241411

2019

dbSNP: rs142346548
rs142346548
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.030 GeneticVariation BEFREE The recently described rs368234815 TT/ΔG dinucleotide and rs117648444 nonsynonymous P70S polymorphisms in IFN lambda 4 (IFNL4) gene, which are strongly associated with response to IFN in hepatitis C virus (HCV) infection, could be also useful in IFN-treated CHB patients. 28732143

2018

dbSNP: rs142346548
rs142346548
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.030 GeneticVariation BEFREE Confounding by Single Nucleotide Polymorphism rs117648444 (P70S) Affects the Association of Interferon Lambda Locus Variants with Response to Interferon-α-Ribavirin Therapy in Patients with Chronic Genotype 3 Hepatitis C Virus Infection. 28727946

2017

dbSNP: rs62120527
rs62120527
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.010 GeneticVariation BEFREE K154E greatly enhanced in vitro activity in a range of antiviral (HCV, Zika virus, influenza virus and encephalomyocarditis virus) and gene expression assays. 30308076

2018