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
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: 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: 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: rs1114167877
rs1114167877
MSH2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553348794
rs1553348794
MSH2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553348842
rs1553348842
MSH2
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1553348882
rs1553348882
MSH2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553348896
rs1553348896
MSH2
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1553348898
rs1553348898
MSH2
ATC 0.700 CausalMutation CLINVAR

dbSNP: rs1553348904
rs1553348904
MSH2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553350466
rs1553350466
MSH2
T 0.700 CausalMutation CLINVAR