Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes. 29967336 2018
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome. 28449805 2017
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 GeneticVariation group CLINVAR Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry Cohort. 29212164 2017
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 GeneticVariation group CLINVAR Thyroid cancer in a patient with Lynch syndrome - case report and literature review. 28769567 2017
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR A molecular inversion probe-based next-generation sequencing panel to detect germline mutations in Chinese early-onset colorectal cancer patients. 28445943 2017
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24 MLH1 and MSH2 Gene Variants. 27629256 2017
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR Multigene Panel Testing Provides a New Perspective on Lynch Syndrome. 28514183 2017
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 GeneticVariation group CLINVAR Elucidating the molecular basis of MSH2-deficient tumors by combined germline and somatic analysis. 28577310 2017
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR MSH2 Loss in Primary Prostate Cancer. 28790115 2017
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 GeneticVariation group CLINVAR Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population. 27601186 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome. 27606285 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR Mutation profiles of synchronous colorectal cancers from a patient with Lynch syndrome suggest distinct oncogenic pathways. 27284491 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR Multilocus Inherited Neoplasia Alleles Syndrome: A Case Series and Review. 26659639 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR Analysis of Lynch Syndrome Mismatch Repair Genes in Women with Endometrial Cancer. 27398995 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group 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
0.900 GeneticVariation group CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer. 26289772 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations. 27064304 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 GeneticVariation group 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
0.900 CausalMutation group CLINVAR Patients with colorectal cancer associated with Lynch syndrome and MLH1 promoter hypermethylation have similar prognoses. 26866578 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population. 27601186 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 CausalMutation group CLINVAR Improving performance of multigene panels for genomic analysis of cancer predisposition. 26845104 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 GeneticVariation group CLINVAR Improving performance of multigene panels for genomic analysis of cancer predisposition. 26845104 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2
0.900 Biomarker group CLINGEN Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer. 27329137 2016