Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1114167845
rs1114167845
MSH2
T 0.700 CausalMutation CLINVAR Simplified identification of Lynch syndrome: a prospective, multicenter study. 22480969

2012
dbSNP: rs1114167845
rs1114167845
MSH2
T 0.700 CausalMutation CLINVAR Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6 in a Greek cohort of Lynch syndrome suspected families. 20937110

2010