Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2596542
rs2596542
Entrez Id: 100507436;101929072
Gene Symbol: MICA;MICA-AS1
MICA;MICA-AS1
CUI: C0019163
Disease:
Hepatitis B
0.020 GeneticVariation BEFREE TT genotype at rs2596542 was a risk factor for the development of HCC in patients with HCV/HBV infection (OR = 1.248, 95% CI: 1.040-1.499, P = 0.017), particularly those with HCV infection (OR = 1.326, 95% CI: 1.101-1.599, P = 0.003) and Asians (OR = 1.273, 95% CI: 1.002-1.618, P = 0.048), or when the control group was patients with chronic hepatitis C (CHC) (OR = 1.506, 95% CI: 1.172-1.936, P = 0.001). 31419949 2019
dbSNP: rs2596542
rs2596542
Entrez Id: 100507436;101929072
Gene Symbol: MICA;MICA-AS1
MICA;MICA-AS1
CUI: C0019163
Disease:
Hepatitis B
0.020 GeneticVariation BEFREE The TT genotype was found to occur more frequently among active HBV carriers (groups II, III and IV) when compared to inactive HBV carriers, thus suggesting that the rs2596542-T may be recessively associated with an active HBV infection. 23994040 2013
dbSNP: rs2523454
rs2523454
Entrez Id: 100507436;101929072
Gene Symbol: MICA;MICA-AS1
MICA;MICA-AS1
CUI: C0019163
Disease:
Hepatitis B
0.010 GeneticVariation BEFREE Our findings suggest that the germline G > A variation at rs2523454 may influence TF-DNA interaction, downregulate the expression of MICA and play an important role in the development of persistent HBV infection in the Chinese population. 31033131 2019