rs12979860, IFNL4

N. diseases: 84
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hepatitis
CUI: C0019158
Disease: Hepatitis
0.040 GeneticVariation BEFREE In the overall analysis, the IL-28B rs12979860 T/C polymorphism was identified as a genetic risk factor for hepatitis virus-related HCC and LC development. 24085431 2013
Hepatitis
CUI: C0019158
Disease: Hepatitis
0.040 GeneticVariation BEFREE In conclusion, the IL28B rs12979860 polymorphism is not associated with fibrosis and liver inflammation in Egyptian HCV G4. 23981065 2014
Hepatitis
CUI: C0019158
Disease: Hepatitis
0.040 GeneticVariation BEFREE The IL28B rs12979860 CC genotype is associated with a higher prevalence of cirrhosis in HIV-HCV-coinfected patients than CT/TT genotypes, suggesting that IL28B CC carriers may experience a more rapid progression of HCV-related liver fibrosis, perhaps as result of increased liver inflammation. 21592993 2011
Hepatitis
CUI: C0019158
Disease: Hepatitis
0.040 GeneticVariation BEFREE The two proposed functional variants (rs368234815 and rs4803217) were not superior to the discovery SNP rs12979860 with respect to liver inflammation or fibrosis phenotype. 28394349 2017