Gene: MSH2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587779973
rs587779973
MSH2
0.700 GeneticVariation UNIPROT Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia. 15996210

2005
dbSNP: rs63749907
rs63749907
MSH2
0.700 GeneticVariation UNIPROT Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia. 15996210

2005
dbSNP: rs63749982
rs63749982
MSH2
0.700 GeneticVariation UNIPROT Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia. 15996210

2005
dbSNP: rs63750006
rs63750006
MSH2
0.700 GeneticVariation UNIPROT Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia. 15996210

2005
dbSNP: rs63750492
rs63750492
MSH2
0.700 GeneticVariation UNIPROT Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia. 15996210

2005
dbSNP: rs63750716
rs63750716
MSH2
0.700 GeneticVariation UNIPROT Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia. 15996210

2005
dbSNP: rs587779973
rs587779973
MSH2
0.700 GeneticVariation UNIPROT Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene. 12792735

2004
dbSNP: rs63749907
rs63749907
MSH2
0.700 GeneticVariation UNIPROT Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene. 12792735

2004
dbSNP: rs63749982
rs63749982
MSH2
0.700 GeneticVariation UNIPROT Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene. 12792735

2004
dbSNP: rs63750006
rs63750006
MSH2
0.700 GeneticVariation UNIPROT Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene. 12792735

2004
dbSNP: rs63750492
rs63750492
MSH2
0.700 GeneticVariation UNIPROT Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene. 12792735

2004
dbSNP: rs63750716
rs63750716
MSH2
0.700 GeneticVariation UNIPROT Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene. 12792735

2004
dbSNP: rs587779973
rs587779973
MSH2
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: rs63749907
rs63749907
MSH2
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: rs63749982
rs63749982
MSH2
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: rs63750006
rs63750006
MSH2
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: rs63750492
rs63750492
MSH2
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: rs63750716
rs63750716
MSH2
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: rs587779973
rs587779973
MSH2
0.700 GeneticVariation UNIPROT Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer. 9559627

1998
dbSNP: rs63749907
rs63749907
MSH2
0.700 GeneticVariation UNIPROT Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer. 9559627

1998
dbSNP: rs63749982
rs63749982
MSH2
0.700 GeneticVariation UNIPROT Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer. 9559627

1998
dbSNP: rs63750006
rs63750006
MSH2
0.700 GeneticVariation UNIPROT Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer. 9559627

1998
dbSNP: rs63750492
rs63750492
MSH2
0.700 GeneticVariation UNIPROT Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer. 9559627

1998
dbSNP: rs63750716
rs63750716
MSH2
0.700 GeneticVariation UNIPROT Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer. 9559627

1998
dbSNP: rs1114167806
rs1114167806
MSH2
T 0.700 CausalMutation CLINVAR