rs1012068, DEPDC5

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
0.800 GeneticVariation GWASCAT Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers. 21725309 2011
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
0.800 GeneticVariation GWASDB Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers. 21725309 2011
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
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
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
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
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
0.760 GeneticVariation BEFREE There was a significant correlation between DEPDC5 rs1012068A/C and HBV-related HCC in the Han Chinese population. 30683632 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
0.760 GeneticVariation BEFREE Recently, the MICA rs2596542 and DEPDC5 rs1012068 variants in Japanese individuals as well as the HCP5 rs2244546 and PNPLA3 rs738409 variants in European individuals have been found associated with hepatocellular carcinoma (HCC). 28928439 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
0.760 GeneticVariation BEFREE In a Northern Italian discovery cohort (n = 477), neither DEPDC5 rs1012068 nor MICA rs2596542 were associated with HCC (n = 150). 26517016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
0.760 GeneticVariation BEFREE Rs423058 upstream of PAPL, rs2834167 in IL10RB and rs1012068 in DEPDC5 were associated with chronic HBV status, HBV natural clearance and the presence of HCC (P = 0.0004–0.024), respectively. 25032264 2014
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
0.760 GeneticVariation BEFREE The data also revealed that subjects with the T allele of both SNPs appeared to have a lower susceptibility to HCV-related cirrhosis/HCC than those with the G allele of rs1012068 (p = 0.038, OR = 1.353, 95 % CI 1.017-1.800) and C allele of rs5998152 (p = 0.043, OR = 1.342, 95 % CI 1.010-1.784). 25551790 2014
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
0.760 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368 2013
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
0.020 GeneticVariation BEFREE However, DEPDC5 rs1012068 was independently associated with cirrhosis (n = 300; P = 0.049). 26517016 2016
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
0.020 GeneticVariation BEFREE However, DEPDC5 rs1012068 was independently associated with cirrhosis (n = 300; P = 0.049). 26517016 2016
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
0.020 GeneticVariation BEFREE Recently, two genetic variants, DEPDC5 rs1012068 and MICA rs2596542, were associated with the onset of HCC in Asian subjects with chronic HCV infection. 26517016 2016
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
0.020 GeneticVariation BEFREE Also, multiple logistic regression analysis showed that rs5998152 (OR = 2.844, 95% CI 1.333-6.069 and p = 0.007), rs1012068 (OR = 2.793, 95% CI 1.316-5.928 and p = 0.010), age (OR = 1.029, 95% CI 1.001-1.057 and p = 0.041) and HCV genotypes (OR = 0.247, 95% CI 0.097-0.630 and p = 0.003) were independently associated with chronicity of HCV infection. 25551790 2014
Cirrhosis
CUI: C1623038
Disease: Cirrhosis
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; 95% 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
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
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