Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs145945630
rs145945630
APC
T 0.700 CausalMutation CLINVAR

dbSNP: rs149633775
rs149633775
TP53
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553125914
rs1553125914
MUTYH
GCT 0.700 GeneticVariation CLINVAR

dbSNP: rs1554085355
rs1554085355
APC
A 0.700 CausalMutation CLINVAR

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 Thus, pooling all related studies did not provide evidence on the association of rs895819 with increased risk of stomach neoplasms. 31669639

2020
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: rs1452231640
rs1452231640
POLB
0.010 GeneticVariation BEFREE Importantly, L22P mice exhibit chronic inflammation accompanied by stomach tumors. 31412651

2019
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