Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs730881815
rs730881815
MSH6 ; FBXO11
T 0.700 CausalMutation CLINVAR Co-occurrence of nonsense mutations in MSH6 and MSH2 in Lynch syndrome families evidencing that not all truncating mutations are equal. 26446363

2016
dbSNP: rs730881815
rs730881815
MSH6 ; FBXO11
T 0.700 CausalMutation CLINVAR MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer. 20924129

2010