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 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
T 0.700 CausalMutation CLINVAR Expanded extracolonic tumor spectrum in MUTYH-associated polyposis. 19732775

2009

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

2009

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

2008

dbSNP: rs36053993
rs36053993
T 0.700 CausalMutation CLINVAR Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors. 11818965

2002

dbSNP: rs104886003
rs104886003
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519044
rs1057519044
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121908382
rs121908382
A 0.700 CausalMutation CLINVAR

dbSNP: rs121908383
rs121908383
C 0.700 CausalMutation CLINVAR

dbSNP: rs121909144
rs121909144
T 0.700 CausalMutation CLINVAR

dbSNP: rs121909775
rs121909775
T 0.700 CausalMutation CLINVAR

dbSNP: rs121909776
rs121909776
C 0.700 CausalMutation CLINVAR

dbSNP: rs121912469
rs121912469
A 0.700 CausalMutation CLINVAR

dbSNP: rs121913279
rs121913279
G 0.700 CausalMutation CLINVAR

dbSNP: rs121913281
rs121913281
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913478
rs121913478
C 0.700 CausalMutation CLINVAR

dbSNP: rs121913530
rs121913530
T 0.700 CausalMutation CLINVAR

dbSNP: rs121918487
rs121918487
T 0.700 CausalMutation CLINVAR

dbSNP: rs121918491
rs121918491
T 0.700 CausalMutation CLINVAR

dbSNP: rs121918505
rs121918505
G 0.700 CausalMutation CLINVAR

dbSNP: rs137854571
rs137854571
APC
T 0.700 CausalMutation CLINVAR

dbSNP: rs137854573
rs137854573
APC
T 0.700 CausalMutation CLINVAR

dbSNP: rs137854575
rs137854575
APC
A 0.700 CausalMutation CLINVAR

dbSNP: rs140342925
rs140342925
T 0.700 CausalMutation CLINVAR

dbSNP: rs1434545235
rs1434545235
C 0.700 CausalMutation CLINVAR