Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28930073
rs28930073
0.720 GeneticVariation UNIPROT Association studies identified a new MLH1 variant (415G-->C, resulting in the amino acid substitution D132H) in approximately 1.3% of Israeli individuals with CRC self-described as Jewish, Christian and Muslim. 15184898

2004

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation UNIPROT DGGE screening of mutations in mismatch repair genes (hMSH2 and hMLH1) in 34 Swedish families with colorectal cancer. 9611074

1998

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation UNIPROT Genetic analysis of familial colorectal cancer in Israeli Arabs. 12655564

2003

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation BEFREE The MLH1 D132H risk variant has significantly lower allele frequency in American compared with Israeli cancer patients and, alone, is unlikely to explain significant amounts of American sporadic colorectal cancer or uterine cancer susceptibility. 15991064

2005

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation UNIPROT Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer. 8872463

1996

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation BEFREE Association studies identified a new MLH1 variant (415G-->C, resulting in the amino acid substitution D132H) in approximately 1.3% of Israeli individuals with CRC self-described as Jewish, Christian and Muslim. 15184898

2004

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation UNIPROT hMLH1 and hMSH2 mutations in families with familial clustering of gastric cancer and hereditary non-polyposis colorectal cancer. 12132870

2001

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation UNIPROT Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer. 18033691

2008

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation UNIPROT Mutational germline analysis of hMSH2 and hMLH1 genes in early onset colorectal cancer patients. 10882759

2000

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation UNIPROT Microsatellite instability and mutation analysis among southern Italian patients with colorectal carcinoma: detection of different alterations accounting for MLH1 and MSH2 inactivation in familial cases. 14504054

2003

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation UNIPROT MSH2 and MLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis. 9087566

1997

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation UNIPROT Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancer. 9032648

1997

dbSNP: rs28930073
rs28930073
0.720 GeneticVariation UNIPROT Missense mutations in hMLH1 associated with colorectal cancer. 10598809

1999

dbSNP: rs267607894
rs267607894
0.700 GeneticVariation UNIPROT Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer. 8872463

1996

dbSNP: rs267607894
rs267607894
0.700 GeneticVariation UNIPROT Genetic analysis of familial colorectal cancer in Israeli Arabs. 12655564

2003

dbSNP: rs267607894
rs267607894
0.700 GeneticVariation UNIPROT MSH2 and MLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis. 9087566

1997

dbSNP: rs267607894
rs267607894
0.700 GeneticVariation UNIPROT Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer. 18033691

2008

dbSNP: rs267607894
rs267607894
0.700 GeneticVariation UNIPROT Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancer. 9032648

1997

dbSNP: rs267607894
rs267607894
0.700 GeneticVariation UNIPROT Microsatellite instability and mutation analysis among southern Italian patients with colorectal carcinoma: detection of different alterations accounting for MLH1 and MSH2 inactivation in familial cases. 14504054

2003

dbSNP: rs267607894
rs267607894
0.700 GeneticVariation UNIPROT hMLH1 and hMSH2 mutations in families with familial clustering of gastric cancer and hereditary non-polyposis colorectal cancer. 12132870

2001

dbSNP: rs267607894
rs267607894
0.700 GeneticVariation UNIPROT DGGE screening of mutations in mismatch repair genes (hMSH2 and hMLH1) in 34 Swedish families with colorectal cancer. 9611074

1998

dbSNP: rs267607894
rs267607894
0.700 GeneticVariation UNIPROT The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer. 15184898

2004

dbSNP: rs267607894
rs267607894
0.700 GeneticVariation UNIPROT Missense mutations in hMLH1 associated with colorectal cancer. 10598809

1999

dbSNP: rs267607894
rs267607894
0.700 GeneticVariation UNIPROT Mutational germline analysis of hMSH2 and hMLH1 genes in early onset colorectal cancer patients. 10882759

2000

dbSNP: rs63749939
rs63749939
0.700 GeneticVariation UNIPROT