Gene: MSH2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060501989
rs1060501989
MSH2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501991
rs1060501991
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: rs1060501991
rs1060501991
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: rs1060501991
rs1060501991
MSH2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501993
rs1060501993
MSH2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501994
rs1060501994
MSH2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502000
rs1060502000
MSH2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502001
rs1060502001
MSH2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502023
rs1060502023
MSH2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1060502027
rs1060502027
MSH2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502029
rs1060502029
MSH2
AAA 0.700 CausalMutation CLINVAR

dbSNP: rs1060502032
rs1060502032
MSH2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502035
rs1060502035
MSH2
GT 0.700 CausalMutation CLINVAR

dbSNP: rs1060502039
rs1060502039
MSH2
G 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: rs1060502039
rs1060502039
MSH2
G 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: rs1064792951
rs1064792951
MSH2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1064793561
rs1064793561
MSH2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1064794155
rs1064794155
MSH2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1064795329
rs1064795329
MSH2
T 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: rs1064795329
rs1064795329
MSH2
T 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: rs1114167805
rs1114167805
MSH2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1114167831
rs1114167831
MSH2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1114167833
rs1114167833
MSH2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1114167841
rs1114167841
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: rs1114167841
rs1114167841
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