Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1054003194
rs1054003194
MSH6 ; FBXO11
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1057517551
rs1057517551
MSH6 ; FBXO11
AT 0.700 CausalMutation CLINVAR

dbSNP: rs1057517763
rs1057517763
MSH6 ; FBXO11
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057517801
rs1057517801
PMS2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057524433
rs1057524433
PMS2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060500687
rs1060500687
MLH1
GA 0.700 CausalMutation CLINVAR

dbSNP: rs1060500688
rs1060500688
MLH1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060500689
rs1060500689
MLH1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060500692
rs1060500692
MLH1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060500703
rs1060500703
MLH1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060500706
rs1060500706
MLH1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060500707
rs1060500707
MLH1
TA 0.700 CausalMutation CLINVAR

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: rs1060502875
rs1060502875
MSH6 ; FBXO11
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060502881
rs1060502881
MSH6 ; FBXO11
G 0.700 CausalMutation CLINVAR