Gene: MSH2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28929483
rs28929483
MSH2
T 0.800 CausalMutation CLINVAR

dbSNP: rs28929484
rs28929484
MSH2
T 0.800 CausalMutation CLINVAR

dbSNP: rs587779067
rs587779067
MSH2
G 0.800 CausalMutation CLINVAR

dbSNP: rs63750070
rs63750070
MSH2
G 0.800 CausalMutation CLINVAR

dbSNP: rs63750126
rs63750126
MSH2
A 0.800 CausalMutation CLINVAR

dbSNP: rs63750214
rs63750214
MSH2
G 0.800 CausalMutation CLINVAR

dbSNP: rs63750398
rs63750398
MSH2
A 0.800 GeneticVariation CLINVAR

dbSNP: rs63750828
rs63750828
MSH2
0.800 GeneticVariation UNIPROT

dbSNP: rs63751207
rs63751207
MSH2
C 0.800 CausalMutation CLINVAR

dbSNP: rs1085308057
rs1085308057
MSH2
0.700 GeneticVariation UNIPROT

dbSNP: rs1114167806
rs1114167806
MSH2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1114167818
rs1114167818
MSH2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1131692279
rs1131692279
MSH2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1194793421
rs1194793421
MSH2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1371291280
rs1371291280
MSH2
0.700 GeneticVariation UNIPROT

dbSNP: rs1553350250
rs1553350250
MSH2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553367635
rs1553367635
MSH2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1558459885
rs1558459885
MSH2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1558466577
rs1558466577
MSH2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1558466685
rs1558466685
MSH2
GC 0.700 GeneticVariation CLINVAR

dbSNP: rs17224367
rs17224367
MSH2
0.700 GeneticVariation UNIPROT

dbSNP: rs267607940
rs267607940
MSH2
A 0.700 CausalMutation CLINVAR

dbSNP: rs267607943
rs267607943
MSH2
C 0.700 CausalMutation CLINVAR

dbSNP: rs267607953
rs267607953
MSH2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs267607969
rs267607969
MSH2
T 0.700 GeneticVariation CLINVAR