Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34612342
rs34612342
MUTYH
C 0.700 CausalMutation CLINVAR Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes. 28944238

2017
dbSNP: rs34612342
rs34612342
MUTYH
C 0.700 CausalMutation CLINVAR Association of monoallelic MUTYH mutation among Egyptian patients with colorectal cancer. 27631816

2017
dbSNP: rs34612342
rs34612342
MUTYH
C 0.700 CausalMutation CLINVAR Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome. 25980754

2015
dbSNP: rs34612342
rs34612342
MUTYH
C 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: rs34612342
rs34612342
MUTYH
C 0.700 CausalMutation CLINVAR A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants. 21063410

2010
dbSNP: rs34612342
rs34612342
MUTYH
C 0.700 CausalMutation CLINVAR Increased colorectal cancer incidence in obligate carriers of heterozygous mutations in MUTYH. 19394335

2009
dbSNP: rs34612342
rs34612342
MUTYH
C 0.700 CausalMutation CLINVAR Analysis of MUTYH genotypes and colorectal phenotypes in patients With MUTYH-associated polyposis. 19032956

2009
dbSNP: rs34612342
rs34612342
MUTYH
C 0.700 CausalMutation CLINVAR Relative and absolute risk of colorectal cancer for individuals with a family history: a meta-analysis. 16338133

2006