Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10020432
rs10020432
AFP
0.010 GeneticVariation BEFREE Furthermore, we identified two SNPs in AFP intron 7 and 3'UTR, rs2298839 and rs10020432, which are associated with increased risk of cirrhosis. 19968979

2010

dbSNP: rs10053538
rs10053538
0.010 GeneticVariation BEFREE This study simultaneously examined PD-1 and TIM-3 expression in liver tissues and PD1 and TIM3 polymorphisms and analyzed their correlations in 171 patients with HBV-related HCC and 34 patients with HBV-related cirrhosis.PD-1 and TIM-3 expression in liver tissues were examined by immunohistochemistry and the genotypes of PD1 rs10204525 and TIM3 rs10053538 polymorphisms were determined using genomic DNA extracted from peripheral blood as template.Both PD-1 and TIM-3 expressions in liver infiltrating lymphocytes of HCC tumor tissues were significantly higher than those in tumor adjacent tissues or cirrhotic tissues. 28033288

2016

dbSNP: rs1012068
rs1012068
0.020 GeneticVariation BEFREE However, DEPDC5 rs1012068 was independently associated with cirrhosis (n = 300; P = 0.049). 26517016

2016

dbSNP: rs1012068
rs1012068
0.020 GeneticVariation BEFREE Also, our results revealed that GT for SNP rs1012068 (OR =1.715; 95% CI 1.132-2.597; p = 0.0104) and CT for SNP rs5998152 (OR = 1.932; 9</span>5% CI 1.276-2.925; p = 0.0017) showed significant association with development of cirrhosis compared with the GG and CC genotypes, respectively. 25551790

2014

dbSNP: rs10146249
rs10146249
0.010 GeneticVariation BEFREE We found three differentially distributed SNPs (rs8021276, rs7158733, and rs10146249) via the screening analysis; however, only rs8021276 polymorphism was further identified to modify the risk of LC. 29937988

2018

dbSNP: rs10204525
rs10204525
0.010 GeneticVariation BEFREE This study simultaneously examined PD-1 and TIM-3 expression in liver tissues and PD1 and TIM3 polymorphisms and analyzed their correlations in 171 patients with HBV-related HCC and 34 patients with HBV-related cirrhosis.PD-1 and TIM-3 expression in liver tissues were examined by immunohistochemistry and the genotypes of PD1 rs10204525 and TIM3 rs10053538 polymorphisms were determined using genomic DNA extracted from peripheral blood as template.Both PD-1 and TIM-3 expressions in liver infiltrating lymphocytes of HCC tumor tissues were significantly higher than those in tumor adjacent tissues or cirrhotic tissues. 28033288

2016

dbSNP: rs1041740
rs1041740
0.010 GeneticVariation BEFREE These data suggest a complex role of SOD1 in different processes leading to complications of liver cirrhosis. rs1041740 might be associated with the development of ascites and possibly plays a role in SBP once ascites has developed. 28403123

2017

dbSNP: rs10433937
rs10433937
0.010 GeneticVariation BEFREE We found that SERPINA1 Pi*S variant conferred an increased risk of developing liver fibrosis, while SERPINA1 Pi*Z and HSD17B13 rs10433937 were not associated with liver fibrosis or cirrhosis of different aetiology. 31517326

2019

dbSNP: rs1049305
rs1049305
0.010 GeneticVariation BEFREE Our results suggest that the rs1049305 (C/G, UTR3) AQP1 polymorphism could be involved in the genetic susceptibility to develop water retention in patients with liver cirrhosis. 21793635

2011

dbSNP: rs1054690270
rs1054690270
0.010 GeneticVariation BEFREE The S267F variant on the NTCP gene is inversely associated with the chronicity of HBV infection, progression to cirrhosis and hepatocellular carcinoma in East Asian populations. 28635613

2018

dbSNP: rs1056836
rs1056836
0.010 GeneticVariation BEFREE Furthermore, high risk for liver cirrhosis-positive clinical status was exhibited in HCC patients with rs1056836 CG and GG genotypes as compared with CC homozygotes. 25796598

2015

dbSNP: rs1059122
rs1059122
0.010 GeneticVariation BEFREE Logistic regression analyses revealed that the risk of liver cirrhosis was significantly higher in subjects with the G/A-G/G genotype of rs3017895 than those with A/A genotype under the dominant model and log additive model, and the T/A-A/A genotype of rs1059122 was positively associated with higher liver cirrhosis than T/T genotype based on dominant model respectively. 30604588

2019

dbSNP: rs10932029
rs10932029
0.010 GeneticVariation BEFREE The rs10932029 genotype "TC" might be an LC-protective factor for HBV genotype C infection. 30600290

2018

dbSNP: rs10945859
rs10945859
0.010 GeneticVariation BEFREE Among these SNPs, CT genotype of rs10945859 was found to have a significant association towards the clinical progression of chronic HCV infection to cirrhosis alone (OR = 1.850; 95% C. I. 27740515

2017

dbSNP: rs11003123
rs11003123
0.010 GeneticVariation BEFREE MBL2 rs11003123 polymorphism may be a marker for the risk of HCC occurrence in patients with HBV-related cirrhosis in the Chinese population. 27298104

2016

dbSNP: rs1127354
rs1127354
0.010 GeneticVariation BEFREE 69 consecutive HCV-1 patients (mean age 57 years) with F3-F4 who received PR and TVR were genotyped for ITPA polymorphisms rs1127354 and rs7270101. 24760000

2014

dbSNP: rs1140409
rs1140409
0.010 GeneticVariation BEFREE We recently identified a missense single nucleotide polymorphism (SNP) in DDX5 (rs1140409, p.S480A) that enhances the risk of developing cirrhosis. 20022962

2010

dbSNP: rs11554495
rs11554495
0.020 GeneticVariation BEFREE In summary, the cytokeratin 8 mutation G61C, which has been found to be associated with cryptogenic liver cirrhosis, was also found in the present patient population. 16911694

2006

dbSNP: rs11554495
rs11554495
0.020 GeneticVariation BEFREE Of the 349 blood bank control samples, only one contained the Tyr-53 --> His and one the Gly-61 --> Cys K8 mutations (P < 0.004 when comparing cirrhosis versus control groups). 12724528

2003

dbSNP: rs1161457931
rs1161457931
0.010 GeneticVariation BEFREE PCSK7 variant rs236918 is a risk factor for cirrhosis in HH patients homozygous for the HFE C282Y mutation. 24556216

2014

dbSNP: rs11614913
rs11614913
0.020 GeneticVariation BEFREE In addition, we found that rs2292832 and rs11614913 were associated with risk of HBV infection, viral clearance and cirrhosis+HCC, whereas rs2910164 was associated with proneness to HBV infection, and ability to clear the virus. 28685993

2017

dbSNP: rs11614913
rs11614913
0.020 GeneticVariation BEFREE The MIR196A2 rs11614913 C > T polymorphism may contribute to an increased risk of HPS in liver cirrhosis patients. 27509319

2017

dbSNP: rs11977021
rs11977021
0.010 GeneticVariation BEFREE In this study, we genotyped two potentially functional single nucleotide polymorphisms (SNPs) in the visfatin promoter region, -1535C>T (rs61330082) and -3187G>A (rs11977021), in 120 HBV-related chronic hepatitis B (CHB) patients, 140 HBV-related liver cirrhosis (HBV-LC) patients, 243 HBV-related hepatocellular carcinoma (HBV-HCC) patients, and 224 asymptomatic HBV carriers. 27792999

2016

dbSNP: rs1201810520
rs1201810520
0.010 GeneticVariation BEFREE The Z variant (Glu342Lys) of α(1)-antitrypsin (AT) polymerizes and accumulates in the hepatocyte endoplasmic reticulum (ER) predisposing to neonatal hepatitis and liver cirrhosis. 22425623

2012

dbSNP: rs12075
rs12075
0.010 GeneticVariation BEFREE Specifically, patients with the <i>DARC</i> rs12075 AG/GG genotype had a lower risk of liver fibrosis progression and development of cirrhosis. 30970632

2019