Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10012
rs10012
CYP1B1 ; CYP1B1-AS1
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 GeneticVariation BEFREE In overall analysis, we found that only the variant G allele of rs1056836 was associated with a significantly increased risk of HCC among the three SNPs (rs10012, rs1056836 and rs1800440). 25796598

2015