Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs36053993
rs36053993
T 0.700 CausalMutation CLINVAR Loss of MUTYH function in human cells leads to accumulation of oxidative damage and genetic instability. 23108399

2013

dbSNP: rs36053993
rs36053993
T 0.700 CausalMutation CLINVAR MUTYH-associated polyposis (MAP): evidence for the origin of the common European mutations p.Tyr179Cys and p.Gly396Asp by founder events. 23361220

2014

dbSNP: rs36053993
rs36053993
T 0.700 CausalMutation CLINVAR Colorectal cancer in a monoallelic MYH mutation carrier. 23625202

2013

dbSNP: rs36053993
rs36053993
T 0.700 CausalMutation CLINVAR Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome. 23805267

2013

dbSNP: rs36053993
rs36053993
T 0.700 CausalMutation CLINVAR Personalized genomic disease risk of volunteers. 24082139

2013

dbSNP: rs36053993
rs36053993
T 0.700 CausalMutation CLINVAR Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing. 24728327

2014