Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.800 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0265325
Disease: Turcot syndrome (disorder)
Turcot syndrome (disorder) 		0.800 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1321489
Disease: Torre-Muir syndrome
Torre-Muir syndrome 		0.800 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.700 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm 		0.700 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.200 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.200 GeneticVariation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.200 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.200 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		0.190 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0037286
Disease: Skin Neoplasms
Skin Neoplasms 		0.180 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0949059
Disease: Polyp of large intestine
Polyp of large intestine 		0.110 GeneticVariation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0034885
Disease: Rectal Neoplasms
Rectal Neoplasms 		0.100 GeneticVariation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0153436
Disease: Malignant neoplasm of sigmoid colon
Malignant neoplasm of sigmoid colon 		0.100 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0153439
Disease: Malignant neoplasm of ascending colon
Malignant neoplasm of ascending colon 		0.100 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0153567
Disease: Uterine Cancer
Uterine Cancer 		0.100 CausalMutation CLINVAR

Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 GeneticVariation CLINVAR Immunosuppression. Binding by design. 1710317

1991
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.130 GeneticVariation CLINVAR Misdiagnosis of the Zollinger-Ellison syndrome due to hyperlipidemia. 2210261

1990
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		0.900 CausalMutation CLINVAR Genetic instability occurs in the majority of young patients with colorectal cancer. 7585065

1995
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C2936783
Disease: Colorectal cancer, hereditary nonpolyposis, type 1
Colorectal cancer, hereditary nonpolyposis, type 1 		0.600 CausalMutation CLINVAR Genetic instability occurs in the majority of young patients with colorectal cancer. 7585065

1995
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.130 CausalMutation CLINVAR Genetic instability occurs in the majority of young patients with colorectal cancer. 7585065

1995
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.130 CausalMutation CLINVAR Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations. 7713503

1994
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.130 CausalMutation CLINVAR Direct mutational analysis in a family with hereditary non-polyposis colorectal cancer. 7717919

1994
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0.130 GeneticVariation CLINVAR Direct mutational analysis in a family with hereditary non-polyposis colorectal cancer. 7717919

1994
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
CUI: C1333990
Disease: Hereditary Nonpolyposis Colorectal Cancer
Hereditary Nonpolyposis Colorectal Cancer 		1.000 CausalMutation CLINVAR Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis. 7726159

1995