Gene: MSH2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 GeneticVariation disease CLINVAR Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database. 24362816 2014
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 CausalMutation disease CLINVAR Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database. 24362816 2014
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 GeneticVariation disease CLINVAR Cancer risk in Lynch Syndrome. 23604856 2013
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 GeneticVariation disease CLINVAR Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. 21642682 2011
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 GeneticVariation disease CLINVAR Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications. 19659756 2009
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 CausalMutation disease CLINVAR Functional analysis of HNPCC-related missense mutations in MSH2. 18822302 2008
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 GeneticVariation disease CLINVAR Concise handbook of familial cancer susceptibility syndromes - second edition. 18559331 2008
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 CausalMutation disease CLINVAR Structure of the human MutSalpha DNA lesion recognition complex. 17531815 2007
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 GeneticVariation disease CLINVAR Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study). 16451135 2006
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 GeneticVariation disease CLINVAR Deletions account for 17% of pathogenic germline alterations in MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer (HNPCC) families. 15943554 2005
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 Biomarker disease BEFREE Recognizing the Lynch 2 syndrome (the existance of multiple HNPCC related cancers in a pedigree), we used polymerase chain reaction followed by direct sequencing to screen the coding regions of both the MSH2 and the MLH1 genes for germline mutations in DNA from the patient. 10874318 2000
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.110 CausalMutation disease CLINVAR Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer. 9774676 1998