Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6078460
rs6078460
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASCAT Genomewide association study for C-reactive protein in Indians replicates known associations of common variants. 30945673

2019

dbSNP: rs584368
rs584368
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASCAT Genomewide association study for C-reactive protein in Indians replicates known associations of common variants. 30945673

2019

dbSNP: rs584368
rs584368
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies a Genetic Prediction Model for Postoperative Survival in Patients with Hepatocellular Carcinoma. 30945699

2019

dbSNP: rs5000634
rs5000634
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368

2013

dbSNP: rs405
rs405
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASDB GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers. 22807686

2012

dbSNP: rs3135363
rs3135363
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368

2013

dbSNP: rs3094137
rs3094137
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASCAT Genome-wide association study identified new susceptible genetic variants in HLA class I region for hepatitis B virus-related hepatocellular carcinoma. 29784950

2018

dbSNP: rs2856723
rs2856723
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASCAT Human leukocyte antigen variants and risk of hepatocellular carcinoma modified by hepatitis C virus genotypes: A genome-wide association study. 28921602

2018

dbSNP: rs2856683
rs2856683
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368

2013

dbSNP: rs2647012
rs2647012
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368

2013

dbSNP: rs17007417
rs17007417
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
T 0.700 GeneticVariation GWASCAT Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers. 29385134

2018

dbSNP: rs10484561
rs10484561
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368

2013

dbSNP: rs8099917
rs8099917
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.090 GeneticVariation BEFREE The T/T genotype of rs8099917 was not associated with the development of HCC (p = 0.623), although stepwise logistic regression analysis showed that liver cirrhosis, age greater than 68 years, and serum albumin <4.2 mg/dl were associated with HCC onset. 22245236

2012

dbSNP: rs8099917
rs8099917
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.090 GeneticVariation BEFREE The results showed that the IL28B rs8099917 AA genotype (AA vs AC + CC: odds ratio (OR) = 0.63, 95 % confidence interval (CI) = 0.46-0.87) was associated with a decreased risk of hepatocellular carcinoma (HCC). 24026885

2014

dbSNP: rs8099917
rs8099917
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.090 GeneticVariation BEFREE Sensitivity analyses suggested the robustness of the results in this meta-analysis.Both IL28B rs12979860 CC and rs8099917 TT genotypes are protective factors for the development of HCC among patients with HBV or HCV infection. 31568008

2019

dbSNP: rs8099917
rs8099917
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.090 GeneticVariation BEFREE In participants with HCV genotype 1, unfavorable genotypes for HCV clearance near IFNL3 were associated with increased HCC risk, the adjusted odds ratio (95% CI) for rs12979860 and rs8099917 being 1.73 (1.00-2.99) and 1.84 (1.02-3.33), respectively. 26602024

2015

dbSNP: rs8099917
rs8099917
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.090 GeneticVariation BEFREE Genotyping of 183 patients with HCC with CHC who were treated with hepatic resection or radiofrequency ablation (RFA) was carried out, and the results were analyzed to determine the association between the IL-28B genotype (rs8099917) and clinical outcome. 23426277

2013

dbSNP: rs8099917
rs8099917
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.090 GeneticVariation BEFREE We genotyped the rs8099917 single-nucleotide polymorphism in 351 hepatitis C-associated HCC patients without history of IFN-based treatment, and correlated the age at onset of HCC in patients with each genotype. 23689989

2014

dbSNP: rs8099917
rs8099917
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.090 GeneticVariation BEFREE rs8099917 nonTT is related to higher HCC development in patients with HCV genotype 1 and those treated with pegylated interferon and ribavirin. 23860735

2014

dbSNP: rs8099917
rs8099917
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.090 GeneticVariation BEFREE To evaluate the role of host IL28B (interleukin 28B; interferon lambda 3) single nucleotide polymorphisms (SNPs) in predicting hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) susceptibility, three SNPs in the IL28B gene (rs12979860C/T, rs8099917G/T and rs12980275G/A) were examined in 330 subjects (including 154 HBV-related HCC patients, 86 non-HCC patients with chronic hepatitis B (CHB), 43 HBV self-limited infections and 47 healthy controls). 22310928

2012

dbSNP: rs8099917
rs8099917
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.090 GeneticVariation BEFREE the Interferon lambda (IFNL) polymorphisms genotypes (rs8099917, rs12979860 and rs12980275) and the presence of mutations in HCV core protein were analyzed in 59 patients with HCC, and also in 50 cirrhotic patients (without HCC). 27035616

2016

dbSNP: rs6025211
rs6025211
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.020 GeneticVariation BEFREE Combinations of single nucleotide polymorphisms WWOX-rs13338697, GALNT14-rs9679162 and rs6025211 effectively stratify outcomes of chemotherapy in advanced hepatocellular carcinoma. 28695683

2018

dbSNP: rs6025211
rs6025211
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.020 GeneticVariation BEFREE Here, we aimed to investigate whether combination of three previously identified single nucleotide polymorphism (SNP) predictors (GALNT14-rs9679162, WWOX-rs13338697, and rs6025211) could guide our choice between systemic chemotherapy, HAIC, and targeted agents in aHCC patients. 31611591

2020

dbSNP: rs12980275
rs12980275
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.020 GeneticVariation BEFREE To evaluate the role of host IL28B (interleukin 28B; interferon lambda 3) single nucleotide polymorphisms (SNPs) in predicting hepatitis B virus (HBV)-related hepatocellular carcinoma (HCC) susceptibility, three SNPs in the IL28B gene (rs12979860C/T, rs8099917G/T and rs12980275G/A) were examined in 330 subjects (including 154 HBV-related HCC patients, 86 non-HCC patients with chronic hepatitis B (CHB), 43 HBV self-limited infections and 47 healthy controls). 22310928

2012

dbSNP: rs12980275
rs12980275
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.020 GeneticVariation BEFREE the rs12980275-AG genotype was associated with HCC on age-adjusted analysis (OR 2.42, 95% CI 1.03-5.69, P=0.043). 27035616

2016