Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes. 9298827 1997
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Novel hMLH1 and hMSH2 germline mutations in African Americans with colorectal cancer. 10386556 1999
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Sixteen rare sequence variants of the hMLH1 and hMSH2 genes found in a cohort of 254 suspected HNPCC (hereditary non-polyposis colorectal cancer) patients: mutations or polymorphisms? 11726306 2001
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Mutations of hMLH1 and hMSH2 in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with microsatellite instability and abnormalities of mismatch repair protein expression. 11870161 2002
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT MSH2 missense mutations and HNPCC syndrome: pathogenicity assessment in a human expression system. 18781619 2008
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia. 15996210 2005
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Genetic characterization of Chinese hereditary non-polyposis colorectal cancer by DHPLC and multiplex PCR. 15613555 2004
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease CLINVAR Integrated analysis of unclassified variants in mismatch repair genes. 21239990 2011
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease CLINVAR Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants. 26951660 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer. 10375096 1999
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Four novel MSH2 / MLH1 gene mutations in portuguese HNPCC families. 10612836 2000
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease CLINVAR Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR). 18383312 2008
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Evaluation of screening strategy for detecting hereditary nonpolyposis colorectal carcinoma. 11920458 2002
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Frequent somatic mutations of hMSH3 with reference to microsatellite instability in hereditary nonpolyposis colorectal cancers. 9240418 1997
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach. 12373605 2002
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT RNA analysis reveals splicing mutations and loss of expression defects in MLH1 and BRCA1. 15300854 2004
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening. 10528862 1999
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. 8261515 1993
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Novel germline mutations of hMSH2 in a patient with hereditary nonpolyposis colorectal cancer (HNPCC) and in a patient with six primary cancers. 9621522 1998
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene. 12658575 2003
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Functional analysis of human MutSalpha and MutSbeta complexes in yeast. 9889267 1999
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 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 		0.600 GeneticVariation disease UNIPROT Functional analysis of HNPCC-related missense mutations in MSH2. 18822302 2008
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer. 15046096 2004
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.600 GeneticVariation disease UNIPROT Population-based molecular detection of hereditary nonpolyposis colorectal cancer. 10829038 2000