Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519824
rs1057519824
MET
CUI: C0007097
Disease: Carcinoma
Carcinoma 		G 0.700 GeneticVariation CLINVAR Novel somatic mutations of the MET oncogene in human carcinoma metastases activating cell motility and invasion. 12460923

2002
dbSNP: rs1057520030
rs1057520030
MET
CUI: C0007097
Disease: Carcinoma
Carcinoma 		T 0.700 GeneticVariation CLINVAR Novel somatic mutations of the MET oncogene in human carcinoma metastases activating cell motility and invasion. 12460923

2002
dbSNP: rs121913245
rs121913245
MET
CUI: C0007097
Disease: Carcinoma
Carcinoma 		C 0.700 GeneticVariation CLINVAR Uncoupling signal transducers from oncogenic MET mutants abrogates cell transformation and inhibits invasive growth. 9826708

1998
dbSNP: rs121913246
rs121913246
MET
CUI: C0007097
Disease: Carcinoma
Carcinoma 		G 0.700 GeneticVariation CLINVAR Uncoupling signal transducers from oncogenic MET mutants abrogates cell transformation and inhibits invasive growth. 9826708

1998
dbSNP: rs121913671
rs121913671
MET
CUI: C0007097
Disease: Carcinoma
Carcinoma 		A 0.700 GeneticVariation CLINVAR Uncoupling signal transducers from oncogenic MET mutants abrogates cell transformation and inhibits invasive growth. 9826708

1998
dbSNP: rs121913671
rs121913671
MET
CUI: C0007097
Disease: Carcinoma
Carcinoma 		C 0.700 GeneticVariation CLINVAR Uncoupling signal transducers from oncogenic MET mutants abrogates cell transformation and inhibits invasive growth. 9826708

1998
dbSNP: rs56391007
rs56391007
MET
CUI: C0007097
Disease: Carcinoma
Carcinoma 		T 0.700 GeneticVariation CLINVAR The radiology of osseous and articular infection. 1104268

1975
dbSNP: rs786202724
rs786202724
MET
CUI: C0007097
Disease: Carcinoma
Carcinoma 		A 0.700 GeneticVariation CLINVAR Novel mutation in the ATP-binding site of the MET oncogene tyrosine kinase in a HPRCC family. 10417759

1999