Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 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: 4292
Gene Symbol: MLH1
MLH1 		0.700 GeneticVariation group CLINVAR Diversity of genetic events associated with MLH1 promoter methylation in Lynch syndrome families with heritable constitutional epimutation. 29790873 2018
Entrez Id: 79728
Gene Symbol: PALB2
PALB2 		0.300 Biomarker group CLINGEN Inherited DNA-Repair Defects in Colorectal Cancer. 29478780 2018
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: 2956
Gene Symbol: MSH6
MSH6 		0.640 GeneticVariation group CLINVAR Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes. 28944238 2017
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 GeneticVariation group CLINVAR Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes. 28944238 2017
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America. 28874130 2017
Entrez Id: 5395
Gene Symbol: PMS2
PMS2 		0.640 CausalMutation group CLINVAR A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America. 28874130 2017
Entrez Id: 79728
Gene Symbol: PALB2
PALB2 		0.300 Biomarker group CLINGEN A pathology atlas of the human cancer transcriptome. 28818916 2017
Entrez Id: 5395
Gene Symbol: PMS2
PMS2 		0.640 CausalMutation group CLINVAR Germline PMS2 and somatic POLE exonuclease mutations cause hypermutability of the leading DNA strand in biallelic mismatch repair deficiency syndrome brain tumours. 28805995 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 Thyroid cancer in a patient with Lynch syndrome - case report and literature review. 28769567 2017
Entrez Id: 4072
Gene Symbol: EPCAM
EPCAM 		0.410 CausalMutation group CLINVAR Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathy. 28701297 2017
Entrez Id: 5395
Gene Symbol: PMS2
PMS2 		0.640 GeneticVariation group CLINVAR DNA mismatch repair deficiency and hereditary syndromes in Latino patients with colorectal cancer. 28640387 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: 2956
Gene Symbol: MSH6
MSH6 		0.640 GeneticVariation group CLINVAR Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity. 28531214 2017
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 GeneticVariation group CLINVAR Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity. 28531214 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: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Multigene Panel Testing Provides a New Perspective on Lynch Syndrome. 28514183 2017
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.640 GeneticVariation group CLINVAR Multigene Panel Testing Provides a New Perspective on Lynch Syndrome. 28514183 2017
Entrez Id: 5395
Gene Symbol: PMS2
PMS2 		0.640 GeneticVariation group CLINVAR Multigene Panel Testing Provides a New Perspective on Lynch Syndrome. 28514183 2017
Entrez Id: 5395
Gene Symbol: PMS2
PMS2 		0.640 CausalMutation group CLINVAR Multigene Panel Testing Provides a New Perspective on Lynch Syndrome. 28514183 2017
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 GeneticVariation group CLINVAR Multigene Panel Testing Provides a New Perspective on Lynch Syndrome. 28514183 2017
Entrez Id: 5395
Gene Symbol: PMS2
PMS2 		0.640 GeneticVariation group CLINVAR Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis? 28503822 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