Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hepatocarcinogenesis
CUI: C1512409
Disease: Hepatocarcinogenesis
0.020 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
Hepatocarcinogenesis
CUI: C1512409
Disease: Hepatocarcinogenesis
0.020 GeneticVariation BEFREE The C allele in MICA rs2596542 is a protective factor for hepatocarcinogenesis, whereas the T allele is a risk factor. 30882647 2019