Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554927408
rs1554927408
FGFR2
T 0.700 CausalMutation CLINVAR

dbSNP: rs28933369
rs28933369
ERBB2 ; MIR4728
A 0.700 CausalMutation CLINVAR

dbSNP: rs28933379
rs28933379
APC
A 0.700 CausalMutation CLINVAR

dbSNP: rs34612342
rs34612342
MUTYH
C 0.700 CausalMutation CLINVAR

dbSNP: rs372267274
rs372267274
MUTYH
G 0.700 CausalMutation CLINVAR

dbSNP: rs397515734
rs397515734
APC
T 0.700 CausalMutation CLINVAR

dbSNP: rs587776802
rs587776802
PIK3CA
GA 0.700 CausalMutation CLINVAR

dbSNP: rs587780088
rs587780088
MUTYH
A 0.700 CausalMutation CLINVAR

dbSNP: rs587781392
rs587781392
APC
T 0.700 CausalMutation CLINVAR

dbSNP: rs587781628
rs587781628
MUTYH
C 0.700 CausalMutation CLINVAR

dbSNP: rs62619935
rs62619935
APC
T 0.700 CausalMutation CLINVAR

dbSNP: rs77543610
rs77543610
FGFR2
C 0.700 CausalMutation CLINVAR

dbSNP: rs786201856
rs786201856
APC
T 0.700 CausalMutation CLINVAR

dbSNP: rs79184941
rs79184941
FGFR2
C 0.700 CausalMutation CLINVAR

dbSNP: rs863225311
rs863225311
APC
G 0.700 GeneticVariation CLINVAR

dbSNP: rs876660765
rs876660765
APC
A 0.700 CausalMutation CLINVAR

dbSNP: rs895819
rs895819
LOC284454 ; MIR23A ; MIR24-2 ; MIR27A
0.020 GeneticVariation BEFREE rs895819 in microRNA-27a increase stomach neoplasms risk in China: A meta-analysis. 31054359

2019
dbSNP: rs36053993
rs36053993
MUTYH
T 0.700 CausalMutation CLINVAR A large-scale meta-analysis to refine colorectal cancer risk estimates associated with MUTYH variants. 21063410

2010
dbSNP: rs36053993
rs36053993
MUTYH
T 0.700 CausalMutation CLINVAR Adenine DNA glycosylase activity of 14 human MutY homolog (MUTYH) variant proteins found in patients with colorectal polyposis and cancer. 20848659

2010
dbSNP: rs36053993
rs36053993
MUTYH
T 0.700 CausalMutation CLINVAR Adenine removal activity and bacterial complementation with the human MutY homologue (MUTYH) and Y165C, G382D, P391L and Q324R variants associated with colorectal cancer. 19836313

2009
dbSNP: rs36053993
rs36053993
MUTYH
T 0.700 CausalMutation CLINVAR Analysis of MUTYH genotypes and colorectal phenotypes in patients With MUTYH-associated polyposis. 19032956

2009
dbSNP: rs36053993
rs36053993
MUTYH
T 0.700 CausalMutation CLINVAR Biallelic MYH germline mutations as cause of Muir-Torre syndrome. 19998059

2010
dbSNP: rs36053993
rs36053993
MUTYH
T 0.700 CausalMutation CLINVAR Cancer-associated variants and a common polymorphism of MUTYH exhibit reduced repair of oxidative DNA damage using a GFP-based assay in mammalian cells. 22926731

2012
dbSNP: rs36053993
rs36053993
MUTYH
T 0.700 CausalMutation CLINVAR Characterization of mutant MUTYH proteins associated with familial colorectal cancer. 18534194

2008
dbSNP: rs36053993
rs36053993
MUTYH
T 0.700 CausalMutation CLINVAR Colorectal cancer in a monoallelic MYH mutation carrier. 23625202

2013