Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918505
rs121918505
FGFR2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1434545235
rs1434545235
FGFR2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554927408
rs1554927408
FGFR2
T 0.700 CausalMutation CLINVAR

dbSNP: rs77543610
rs77543610
FGFR2
C 0.700 CausalMutation CLINVAR

dbSNP: rs79184941
rs79184941
FGFR2
C 0.700 CausalMutation CLINVAR

dbSNP: rs121912469
rs121912469
IRF1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121909144
rs121909144
KLF6
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913529
rs121913529
KRAS
T 0.710 CausalMutation CLINVAR

dbSNP: rs121913529
rs121913529
KRAS
0.710 GeneticVariation BEFREE One case had a KRAS G12V (c.35G>T) mutation in both the primary gastric tumor and a post-imatinib recurrence. 25427437

2015
dbSNP: rs121913530
rs121913530
KRAS
T 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: rs895819
rs895819
LOC284454 ; MIR23A ; MIR24-2 ; MIR27A
0.020 GeneticVariation BEFREE Thus, pooling all related studies did not provide evidence on the association of rs895819 with increased risk of stomach neoplasms. 31669639

2020
dbSNP: rs121908382
rs121908382
MUTYH
A 0.700 CausalMutation CLINVAR

dbSNP: rs121908383
rs121908383
MUTYH
C 0.700 CausalMutation CLINVAR

dbSNP: rs140342925
rs140342925
MUTYH
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553125914
rs1553125914
MUTYH
GCT 0.700 GeneticVariation CLINVAR

dbSNP: rs34612342
rs34612342
MUTYH
C 0.700 CausalMutation CLINVAR

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

2002
dbSNP: rs36053993
rs36053993
MUTYH
T 0.700 CausalMutation CLINVAR Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes. 22703879

2012
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 Functional analysis of MUTYH mutated proteins associated with familial adenomatous polyposis. 20418187

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 Expanded extracolonic tumor spectrum in MUTYH-associated polyposis. 19732775

2009
dbSNP: rs36053993
rs36053993
MUTYH
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
MUTYH
T 0.700 CausalMutation CLINVAR Germline variation in cancer-susceptibility genes in a healthy, ancestrally diverse cohort: implications for individual genome sequencing. 24728327

2014