Gene: MLH1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060500688
rs1060500688
MLH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1064795441
rs1064795441
MLH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1416171624
rs1416171624
MLH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1434898623
rs1434898623
MLH1
A 0.700 CausalMutation CLINVAR Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome. 21642682

2011
dbSNP: rs1434898623
rs1434898623
MLH1
A 0.700 CausalMutation CLINVAR Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer. 15713769

2005
dbSNP: rs1434898623
rs1434898623
MLH1
A 0.700 CausalMutation CLINVAR Mutation spectrum and risk of colorectal cancer in African American families with Lynch syndrome. 26248088

2015
dbSNP: rs1434898623
rs1434898623
MLH1
A 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: rs1553645226
rs1553645226
MLH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553647894
rs1553647894
MLH1
A 0.700 GeneticVariation CLINVAR UMD (Universal mutation database): a generic software to build and analyze locus-specific databases. 10612827

2000
dbSNP: rs1553647894
rs1553647894
MLH1
A 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: rs1553647894
rs1553647894
MLH1
A 0.700 GeneticVariation CLINVAR Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer. 15713769

2005
dbSNP: rs1553648023
rs1553648023
MLH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1559524070
rs1559524070
MLH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs267607717
rs267607717
MLH1
A 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: rs267607717
rs267607717
MLH1
A 0.700 CausalMutation CLINVAR Mismatch repair gene mutations in Chinese HNPCC patients. 18931482

2008
dbSNP: rs267607717
rs267607717
MLH1
A 0.700 CausalMutation CLINVAR Mutation spectrum in HNPCC in the Israeli population. 18389388

2008
dbSNP: rs267607717
rs267607717
MLH1
A 0.700 CausalMutation CLINVAR Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population. 27601186

2016
dbSNP: rs267607717
rs267607717
MLH1
A 0.700 CausalMutation CLINVAR Candidate colorectal cancer predisposing gene variants in Chinese early-onset and familial cases. 25892863

2015
dbSNP: rs267607717
rs267607717
MLH1
A 0.700 CausalMutation CLINVAR Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer. 15713769

2005
dbSNP: rs267607718
rs267607718
MLH1
A 0.700 GeneticVariation CLINVAR Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer. 15713769

2005
dbSNP: rs267607718
rs267607718
MLH1
A 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: rs267607725
rs267607725
MLH1
A 0.700 GeneticVariation CLINVAR Classification of mismatch repair gene missense variants with PON-MMR. 22290698

2012
dbSNP: rs267607734
rs267607734
MLH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs267607744
rs267607744
MLH1
A 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: rs267607744
rs267607744
MLH1
A 0.700 GeneticVariation CLINVAR Mutation spectrum and risk of colorectal cancer in African American families with Lynch syndrome. 26248088

2015