Disease: Neoplastic Syndromes, Hereditary ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913670
rs121913670
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		A 0.700 CausalMutation CLINVAR The HSP90 inhibitor ganetespib synergizes with the MET kinase inhibitor crizotinib in both crizotinib-sensitive and -resistant MET-driven tumor models. 24121490 2013
dbSNP: rs121913670
rs121913670
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		A 0.700 CausalMutation CLINVAR The novel ATP-competitive inhibitor of the MET hepatocyte growth factor receptor EMD1214063 displays inhibitory activity against selected MET-mutated variants. 24061647 2013
dbSNP: rs121913670
rs121913670
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		A 0.700 CausalMutation CLINVAR Novel mutations of the MET proto-oncogene in papillary renal carcinomas. 10327054 1999
dbSNP: rs121913670
rs121913670
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		A 0.700 CausalMutation CLINVAR Activating mutations for the met tyrosine kinase receptor in human cancer. 9326629 1997
dbSNP: rs121913670
rs121913670
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		A 0.700 CausalMutation CLINVAR Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas. 9140397 1997