Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5395
Gene Symbol: PMS2
PMS2 		0.640 GeneticVariation group CLINVAR [Retrospective NGS Study in High-risk Hereditary Cancer Patients at Masaryk Memorial Cancer Institute]. 26691941 2016
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR [Founder mutation in Lynch syndrome]. 27295708 2016
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 GeneticVariation group LHGDN [Familial and genetic study in a large Chinese kindred with hereditary nonpolyposis colorectal cancer]. 17407090 2007
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.640 GeneticVariation group CLINVAR [Constitutional mismatch repair deficiency syndrome]. 26200421 2015
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 GeneticVariation group CLINVAR [Constitutional mismatch repair deficiency syndrome]. 26200421 2015
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 GeneticVariation group LHGDN [Comparison of clinical and genetic phenotypes between Chinese and Korean hereditary nonpolyposis colorectal cancer families]. 18543228 2008
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 GeneticVariation group LHGDN [Comparison of clinical and genetic phenotypes between Chinese and Korean hereditary nonpolyposis colorectal cancer families]. 18543228 2008
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 GeneticVariation group LHGDN [Clinical features and hMSH2/hMLH1 germline mutation screening of Chinese hereditary nonpolyposis colorectal cancer patients]. 15200905 2004
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 GeneticVariation group LHGDN [Clinical features and hMSH2/hMLH1 germline mutation screening of Chinese hereditary nonpolyposis colorectal cancer patients]. 15200905 2004
Entrez Id: 4436
Gene Symbol: MSH2
MSH2 		0.900 AlteredExpression group LHGDN [Clinical analysis and molecular genetic study of hereditary nonpolyposis colorectal cancer kindreds]. 15062061 2004
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 AlteredExpression group LHGDN [Clinical analysis and molecular genetic study of hereditary nonpolyposis colorectal cancer kindreds]. 15062061 2004
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR [A method of study for stomatological materials]. 1061282 1976
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.640 CausalMutation group CLINVAR Yield of routine molecular analyses in colorectal cancer patients ≤70 years to detect underlying Lynch syndrome. 22081473 2012
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 CausalMutation group CLINVAR Yield of routine molecular analyses in colorectal cancer patients ≤70 years to detect underlying Lynch syndrome. 22081473 2012
Entrez Id: 2052
Gene Symbol: EPHX1
EPHX1 		0.300 Biomarker group CLINGEN Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer. 25058500 2015
Entrez Id: 64332
Gene Symbol: NFKBIZ
NFKBIZ 		0.300 Biomarker group CLINGEN Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer. 25058500 2015
Entrez Id: 6597
Gene Symbol: SMARCA4
SMARCA4 		0.300 Biomarker group CLINGEN Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer. 25058500 2015
Entrez Id: 580
Gene Symbol: BARD1
BARD1 		0.300 Biomarker group CLINGEN Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer. 25058500 2015
Entrez Id: 1027
Gene Symbol: CDKN1B
CDKN1B 		0.300 Biomarker group CLINGEN Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer. 25058500 2015
Entrez Id: 7518
Gene Symbol: XRCC4
XRCC4 		0.300 Biomarker group CLINGEN Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer. 25058500 2015
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 GeneticVariation group CLINVAR What scientists would like to tell you about reprogramming (if only they knew!). Preface. 21404177 2010
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.640 CausalMutation group CLINVAR Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability. 17117178 2006
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.100 CausalMutation group CLINVAR Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability. 17117178 2006
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 CausalMutation group CLINVAR Verification of the three-step model in assessing the pathogenicity of mismatch repair gene variants. 21120944 2011
Entrez Id: 4292
Gene Symbol: MLH1
MLH1 		0.700 GeneticVariation group CLINVAR Verification of the three-step model in assessing the pathogenicity of mismatch repair gene variants. 21120944 2011