Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913675
rs121913675
MET
CUI: C0279606
Disease: Childhood Hepatocellular Carcinoma
Childhood Hepatocellular Carcinoma 		T 0.700 CausalMutation CLINVAR

dbSNP: rs121913676
rs121913676
MET
CUI: C0279606
Disease: Childhood Hepatocellular Carcinoma
Childhood Hepatocellular Carcinoma 		A 0.700 CausalMutation CLINVAR

dbSNP: rs121913677
rs121913677
MET
CUI: C0279606
Disease: Childhood Hepatocellular Carcinoma
Childhood Hepatocellular Carcinoma 		G 0.700 CausalMutation CLINVAR