Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs759680369
rs759680369
MLH1 ; EPM2AIP1
A 0.700 GeneticVariation CLINVAR Diversity of genetic events associated with MLH1 promoter methylation in Lynch syndrome families with heritable constitutional epimutation. 29790873

2018
dbSNP: rs759680369
rs759680369
MLH1 ; EPM2AIP1
A 0.700 GeneticVariation CLINVAR Identification of constitutional MLH1 epimutations and promoter variants in colorectal cancer patients from the Colon Cancer Family Registry. 22878509

2013