Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs143353451
rs143353451
MUTYH
T 0.700 CausalMutation CLINVAR Inherited DNA-Repair Defects in Colorectal Cancer. 29478780

2018
dbSNP: rs143353451
rs143353451
MUTYH
T 0.700 CausalMutation CLINVAR Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer. 28135145

2017
dbSNP: rs143353451
rs143353451
MUTYH
T 0.700 CausalMutation CLINVAR Functional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain. 25820570

2015
dbSNP: rs143353451
rs143353451
MUTYH
T 0.700 CausalMutation CLINVAR Impaired suppressive activities of human MUTYH variant proteins against oxidative mutagenesis. 23322991

2012
dbSNP: rs143353451
rs143353451
MUTYH
T 0.700 CausalMutation CLINVAR MUTYH-associated polyposis - variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations. 20618354

2010