Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 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: rs1057519891
rs1057519891
ERBB3
0.010 GeneticVariation BEFREE The D297Y mutation was previously detected in breast and gastric tumors, but not in CRC. 26287187

2015
dbSNP: rs1131691021
rs1131691021
TP53
0.010 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: rs1342376116
rs1342376116
ARID1A
0.010 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: rs1431341935
rs1431341935
SORD
0.010 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: rs1440200916
rs1440200916
PDGFRA
0.010 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: rs1440200916
rs1440200916
PDGFRA
0.010 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: rs1452231640
rs1452231640
POLB
0.010 GeneticVariation BEFREE Importantly, L22P mice exhibit chronic inflammation accompanied by stomach tumors. 31412651

2019
dbSNP: rs762846821
rs762846821
TP53
0.010 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: rs104886003
rs104886003
PIK3CA
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519803
rs1057519803
ERBB3
A 0.700 GeneticVariation CLINVAR Oncogenic ERBB3 mutations in human cancers. 23680147

2013
dbSNP: rs121908382
rs121908382
MUTYH
A 0.700 CausalMutation CLINVAR

dbSNP: rs121912469
rs121912469
IRF1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121913403
rs121913403
CTNNB1
A 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs137854575
rs137854575
APC
A 0.700 CausalMutation CLINVAR

dbSNP: rs149633775
rs149633775
TP53
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554085355
rs1554085355
APC
A 0.700 CausalMutation CLINVAR

dbSNP: rs28933369
rs28933369
ERBB2 ; MIR4728
A 0.700 CausalMutation CLINVAR

dbSNP: rs28933379
rs28933379
APC
A 0.700 CausalMutation CLINVAR

dbSNP: rs587780088
rs587780088
MUTYH
A 0.700 CausalMutation CLINVAR

dbSNP: rs876660765
rs876660765
APC
A 0.700 CausalMutation CLINVAR

dbSNP: rs121908383
rs121908383
MUTYH
C 0.700 CausalMutation CLINVAR

dbSNP: rs121909776
rs121909776
CASP10
C 0.700 CausalMutation CLINVAR