Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12476364
rs12476364
MSH2
A 0.700 CausalMutation CLINVAR Patients with colorectal cancer associated with Lynch syndrome and MLH1 promoter hypermethylation have similar prognoses. 26866578

2016
dbSNP: rs12476364
rs12476364
MSH2
T 0.700 CausalMutation CLINVAR Patients with colorectal cancer associated with Lynch syndrome and MLH1 promoter hypermethylation have similar prognoses. 26866578

2016
dbSNP: rs12476364
rs12476364
MSH2
T 0.700 CausalMutation 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
dbSNP: rs12476364
rs12476364
MSH2
C 0.700 GeneticVariation 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
dbSNP: rs12476364
rs12476364
MSH2
A 0.700 CausalMutation CLINVAR Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer. 15849733

2005
dbSNP: rs12476364
rs12476364
MSH2
T 0.700 CausalMutation CLINVAR Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer. 15849733

2005
dbSNP: rs12476364
rs12476364
MSH2
C 0.700 GeneticVariation CLINVAR Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer. 15849733

2005
dbSNP: rs12476364
rs12476364
MSH2
T 0.700 CausalMutation CLINVAR Economic and Practical Factors in Diagnosing HNPCC Using Clinical Criteria, Immunohistochemistry and Microsatellite Instability Analysis. 20233461

2004
dbSNP: rs12476364
rs12476364
MSH2
A 0.700 CausalMutation CLINVAR Economic and Practical Factors in Diagnosing HNPCC Using Clinical Criteria, Immunohistochemistry and Microsatellite Instability Analysis. 20233461

2004
dbSNP: rs12476364
rs12476364
MSH2
A 0.700 CausalMutation CLINVAR Clinical consequences of molecular diagnosis in families with mismatch repair gene germline mutations. 11151427

2000
dbSNP: rs12476364
rs12476364
MSH2
T 0.700 CausalMutation CLINVAR Clinical consequences of molecular diagnosis in families with mismatch repair gene germline mutations. 11151427

2000