Gene: MSH2 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1114167806
rs1114167806
MSH2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553368590
rs1553368590
MSH2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs587779157
rs587779157
MSH2
G 0.700 CausalMutation CLINVAR

dbSNP: rs63751207
rs63751207
MSH2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs869312768
rs869312768
MSH2
CTT 0.700 CausalMutation CLINVAR