Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786201066
rs786201066
MSH2
T 0.700 CausalMutation CLINVAR Screening for Lynch syndrome in colorectal cancer: are we doing enough? 21879275

2012
dbSNP: rs786201066
rs786201066
MSH2
T 0.700 CausalMutation CLINVAR Cancer risk in 348 French MSH2 or MLH1 gene carriers. 12624141

2003