Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28934571
rs28934571
0.800 GeneticVariation BEFREE Co-targeting p53-R249S and CDK4 synergistically suppresses survival of hepatocellular carcinoma cells. 31747859

2020

dbSNP: rs25487
rs25487
0.100 GeneticVariation BEFREE Our study indicated that the XRCC1 rs25487 was a risk factor for the susceptibility of HCC, which was verified by the TSA. 31478224

2020

dbSNP: rs25489
rs25489
0.100 GeneticVariation BEFREE In addition, the rs25489 and rs1799782 polymorphisms were associated with increased risk of HCC. 31478224

2020

dbSNP: rs1799782
rs1799782
0.070 GeneticVariation BEFREE In addition, the rs25489 and rs1799782 polymorphisms were associated with increased risk of HCC. 31478224

2020

dbSNP: rs9679162
rs9679162
0.060 GeneticVariation BEFREE A GALNT14 rs9679162 genotype-guided therapeutic strategy for advanced hepatocellular carcinoma: systemic or hepatic arterial infusion chemotherapy. 31611591

2020

dbSNP: rs1695
rs1695
0.030 GeneticVariation BEFREE Herein, we investigated the relationship of three GSTs polymorphisms (GSTT1 deletion, GSTM1 deletion, GSTP1 rs1695) as well as GSTP1 promoter region DNA methylation and HCC risk with a particular focus on the interaction with OCPs exposure among 90 HCC cases and 99 controls in a Chinese population. 31731000

2020

dbSNP: rs72613567
rs72613567
0.030 GeneticVariation BEFREE We tested the association of rs72613567 with plasma levels of alanine transaminase (ALT) and clinical liver disease and mortality in 111,612 individuals from the Danish general population, including 497 with cirrhosis and 113 with hepatocellular carcinoma. 31155741

2020

dbSNP: rs6025211
rs6025211
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: rs7975232
rs7975232
VDR
0.020 GeneticVariation BEFREE Apa1 (rs7975232) SNP in the vitamin D receptor is linked to hepatocellular carcinoma in hepatitis C virus cirrhosis. 31682785

2020

dbSNP: rs920778
rs920778
0.020 GeneticVariation BEFREE A single nucleotide polymorphism (SNP) rs920778 in the HOTAIR gene, has been recurrently studied for susceptibility to many cancers including oesophageal cancer, gastric cancer, lung cancer, and hepatocellular carcinoma. 31759985

2020

dbSNP: rs2844512
rs2844512
0.010 GeneticVariation BEFREE The rs2844512 G > C variant in LINC01149 was identified to facilitate HBV spontaneous recovery (OR = 0.84, 95% CI = 0.77-0.92) but increase the risk of HCC (OR = 1.21, 95% CI = 1.11-1.32) in combined samples. 31754211

2020

dbSNP: rs34000982
rs34000982
0.010 GeneticVariation BEFREE These data suggest that the rs34000982 polymorphism may contribute to HCC susceptibility, in full or at least partially through the effect on HMGB1 transcriptional activity by disturbing the binding of miR-636 with the 3'UTR of HMGB1. 31777261

2020

dbSNP: rs17401966
rs17401966
0.900 GeneticVariation BEFREE More well-designed studies with larger sample size and various ethnic groups and risk factors are needed to establish that KIF1B rs17401966 polymorphism is significantly associated with risk of HCC. 30947687

2019

dbSNP: rs2596542
rs2596542
0.900 GeneticVariation BEFREE However, genotype frequencies of rs2596542A/G SNP were statistically different between HCV-induced HCC patients and controls (p = 0.048), and also between HCC and HCV-induced cirrhosis patients (p = 0.039). 31471884

2019

dbSNP: rs2596542
rs2596542
0.900 GeneticVariation BEFREE The findings of this meta-analysis suggest that the rs2596542 variant in the MICA promoter region may affect MICA and soluble MICA (sMICA) protein expression, thereby influencing physiological vulnerability to HCC cells and the development of HCC. 31419949

2019

dbSNP: rs2596542
rs2596542
0.900 GeneticVariation BEFREE Recently, two GWAS variants, MICA rs2596542 and DEPDC5 rs1012068 were identified as being associated with the development of HCV-induced hepatocellular carcinoma (HCC) in Japanese patients. 30723271

2019

dbSNP: rs2596542
rs2596542
0.900 GeneticVariation BEFREE Nevertheless, we also detected significant associations between rs259</span>6542G>A and HCV-induced HCC</span>. 30967497

2019

dbSNP: rs2596542
rs2596542
0.900 GeneticVariation BEFREE A meta-analysis was performed to examine the association between MICA rs2596542 polymorphism and susceptibility to HCC. 30882647

2019

dbSNP: rs2596542
rs2596542
0.900 GeneticVariation BEFREE Taken together our study suggest that MICA rs2596542 SNP impacts HCV-induced HCC susceptibility suggesting that genetic variants in MICA are of clinical relevance to hepatocarcinogenesis by impacting host immune response in chronic HCV infection. 31471884

2019

dbSNP: rs7574865
rs7574865
0.900 GeneticVariation BEFREE The present study also indicates that <i>STAT4</i> rs7574865 polymorphism increased the risk of chronic HBV infection and HCC. 31160486

2019

dbSNP: rs7574865
rs7574865
0.900 GeneticVariation BEFREE In contrast, STAT4-rs7574865 was associated with HCC only in HBV infected patients (p = 0.03) and the other tested SNP were not linked with HCC risk. 30289982

2019

dbSNP: rs28934571
rs28934571
0.800 GeneticVariation BEFREE This review will discuss these findings as well as their clinical significance and implications for the development of a strategy to target multiple molecules as a therapy for p53-R249S-harboring HCC. 30608603

2019

dbSNP: rs1012068
rs1012068
0.760 GeneticVariation BEFREE Recently, two GWAS variants, MICA rs2596542 and DEPDC5 rs1012068 were identified as being associated with the development of HCV-induced hepatocellular carcinoma (HCC) in Japanese patients. 30723271

2019

dbSNP: rs1012068
rs1012068
0.760 GeneticVariation BEFREE After controlling for the influence of sex, smoking and drinking, this study showed a significant relationship between the polymorphism of DEPDC5 rs1012068 and HBV-related HCC. 30683632

2019

dbSNP: rs1012068
rs1012068
0.760 GeneticVariation BEFREE There was a significant correlation between DEPDC5 rs1012068A/C and HBV-related HCC in the Han Chinese population. 30683632

2019