Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913675
rs121913675
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0279606
Disease:
Childhood Hepatocellular Carcinoma
T 0.700 CausalMutation CLINVAR
dbSNP: rs121913676
rs121913676
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0279606
Disease:
Childhood Hepatocellular Carcinoma
A 0.700 CausalMutation CLINVAR
dbSNP: rs121913677
rs121913677
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0279606
Disease:
Childhood Hepatocellular Carcinoma
G 0.700 CausalMutation CLINVAR