Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12564469
rs12564469
Entrez Id: 26038
Gene Symbol: CHD5
CHD5
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE We discovered a rare variant (haplotype AG) in CHD5 (rs12564469-rs9434711) that was markedly associated with the risk of HCC in a Chinese population. 29907144 2018
dbSNP: rs9434711
rs9434711
Entrez Id: 26038
Gene Symbol: CHD5
CHD5
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE We discovered a rare variant (haplotype AG) in CHD5 (rs12564469-rs9434711) that was markedly associated with the risk of HCC in a Chinese population. 29907144 2018