Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs794728016
rs794728016
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C4084709
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 97 		0.800 GeneticVariation UNIPROT
dbSNP: rs794728016
rs794728016
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C4084709
Disease:
DEAFNESS, AUTOSOMAL RECESSIVE 97 		G 0.800 CausalMutation CLINVAR
dbSNP: rs121913243
rs121913243
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0007134
Disease:
Renal Cell Carcinoma 		G 0.700 CausalMutation CLINVAR
dbSNP: rs121913246
rs121913246
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0007134
Disease:
Renal Cell Carcinoma 		G 0.700 CausalMutation CLINVAR
dbSNP: rs121913669
rs121913669
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0007134
Disease:
Renal Cell Carcinoma 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121913670
rs121913670
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0007134
Disease:
Renal Cell Carcinoma 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121913671
rs121913671
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0007134
Disease:
Renal Cell Carcinoma 		A 0.700 CausalMutation CLINVAR
dbSNP: rs121913673
rs121913673
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0007134
Disease:
Renal Cell Carcinoma 		G 0.700 CausalMutation CLINVAR
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
dbSNP: rs1554400286
rs1554400286
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0220662
Disease:
ARTHROGRYPOSIS, DISTAL, TYPE 1 		G 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs768678989
rs768678989
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.700 GeneticVariation UNIPROT
dbSNP: rs771333219
rs771333219
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.700 GeneticVariation UNIPROT
dbSNP: rs786202724
rs786202724
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0007134
Disease:
Renal Cell Carcinoma 		A 0.700 CausalMutation CLINVAR
dbSNP: rs869320706
rs869320706
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C4085248
Disease:
OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO 		C 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs869320707
rs869320707
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C4085248
Disease:
OSTEOFIBROUS DYSPLASIA, SUSCEPTIBILITY TO 		T 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs794728016
rs794728016
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C3874334
Disease:
Severe hearing loss 		G 0.700 CausalMutation CLINVAR A mutation of MET, encoding hepatocyte growth factor receptor, is associated with human DFNB97 hearing loss. 25941349 2015
dbSNP: rs121913243
rs121913243
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C1336839
Disease:
Type 1 Papillary Renal Cell Carcinoma 		0.700 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
dbSNP: rs121913246
rs121913246
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C1336839
Disease:
Type 1 Papillary Renal Cell Carcinoma 		0.700 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
dbSNP: rs121913668
rs121913668
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C1336839
Disease:
Type 1 Papillary Renal Cell Carcinoma 		0.700 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
dbSNP: rs121913669
rs121913669
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C1336839
Disease:
Type 1 Papillary Renal Cell Carcinoma 		0.700 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
dbSNP: rs121913670
rs121913670
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C1336839
Disease:
Type 1 Papillary Renal Cell Carcinoma 		0.700 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
dbSNP: rs121913673
rs121913673
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C1336839
Disease:
Type 1 Papillary Renal Cell Carcinoma 		0.700 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
dbSNP: rs121913668
rs121913668
Entrez Id: 4233
Gene Symbol: MET
MET
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		C 0.700 CausalMutation CLINVAR Activating mutations for the met tyrosine kinase receptor in human cancer. 9326629 1997