Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes. 28944238 2017
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Tumor testing to identify lynch syndrome in two Australian colorectal cancer cohorts. 27273229 2017
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312 2016
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population. 27601186 2016
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312 2016
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Germline multi-gene hereditary cancer panel testing in an unselected endometrial cancer cohort. 27443514 2016
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Inherited Mutations in Women With Ovarian Carcinoma. 26720728 2016
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. 25980754 2015
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing. 25559809 2015
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Characterization of a novel founder MSH6 mutation causing Lynch syndrome in the French Canadian population. 25318681 2015
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Combined Microsatellite Instability, MLH1 Methylation Analysis, and Immunohistochemistry for Lynch Syndrome Screening in Endometrial Cancers From GOG210: An NRG Oncology and Gynecologic Oncology Group Study. 26552419 2015
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing. 25559809 2015
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Identification of germline genetic mutations in patients with pancreatic cancer. 26440929 2015
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR The gastrointestinal manifestation of constitutional mismatch repair deficiency syndrome: from a single adenoma to polyposis-like phenotype and early onset cancer. 25307252 2015
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. 25980754 2015
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population. 24728189 2014
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 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: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population. 24728189 2014
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. 24763289 2014
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the constitutional mismatch repair deficiency consortium. 24440087 2014
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 Biomarker disease GENOMICS_ENGLAND 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: 2956
Gene Symbol: MSH6
MSH6 		0.700 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: 2956
Gene Symbol: MSH6
MSH6 		0.700 CausalMutation disease CLINVAR A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry. 22949379 2013
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR Population-based molecular screening for Lynch syndrome: implications for personalized medicine. 23733757 2013
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.700 GeneticVariation disease CLINVAR A multifactorial likelihood model for MMR gene variant classification incorporating probabilities based on sequence bioinformatics and tumor characteristics: a report from the Colon Cancer Family Registry. 22949379 2013