Gene: MLH1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060500699
rs1060500699
MLH1
GT 0.700 CausalMutation CLINVAR

dbSNP: rs1064795515
rs1064795515
MLH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1064795693
rs1064795693
MLH1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1302248679
rs1302248679
MLH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1305605404
rs1305605404
MLH1
G 0.700 GeneticVariation CLINVAR Structure of the human MLH1 N-terminus: implications for predisposition to Lynch syndrome. 26249686

2015
dbSNP: rs1416171624
rs1416171624
MLH1
A 0.700 CausalMutation CLINVAR Tumor microsatellite instability in early onset gastric cancer. 16237216

2005
dbSNP: rs1416171624
rs1416171624
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 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 Mutation spectrum and risk of colorectal cancer in African American families with Lynch syndrome. 26248088

2015
dbSNP: rs1437454428
rs1437454428
MLH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553637196
rs1553637196
MLH1 ; EPM2AIP1
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1553640334
rs1553640334
MLH1
C 0.700 GeneticVariation CLINVAR Distinctive patterns of p53 protein expression and microsatellite instability in human colorectal cancer. 21665242

2011
dbSNP: rs1553641295
rs1553641295
MLH1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553642718
rs1553642718
MLH1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553642777
rs1553642777
MLH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553644123
rs1553644123
MLH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553645301
rs1553645301
MLH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553645331
rs1553645331
MLH1
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1553646764
rs1553646764
MLH1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553647969
rs1553647969
MLH1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553648040
rs1553648040
MLH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553648068
rs1553648068
MLH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553648149
rs1553648149
MLH1
G 0.700 CausalMutation CLINVAR Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer. 15713769

2005
dbSNP: rs1553650741
rs1553650741
MLH1
TA 0.700 CausalMutation CLINVAR

dbSNP: rs1553651299
rs1553651299
MLH1
TGCTGAAGTGGCT 0.700 CausalMutation CLINVAR