rs895819
|
|
|
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 |
rs1057519891
|
|
|
0.010 |
GeneticVariation |
BEFREE |
The D297Y mutation was previously detected in breast and gastric tumors, but not in CRC.
|
26287187 |
2015 |
rs36053993
|
|
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 |
rs36053993
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Rectum-sparing surgery may be appropriate for biallelic MutYH-associated polyposis.
|
21178863 |
2010 |
rs1057519836
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
rs121434595
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
rs121913228
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
rs121913403
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Prospective enterprise-level molecular genotyping of a cohort of cancer patients.
|
25157968 |
2014 |
rs36053993
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Personalized genomic disease risk of volunteers.
|
24082139 |
2013 |
rs1342376116
|
|
|
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 |
rs1131691021
|
|
|
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 |
rs1431341935
|
|
|
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 |
rs1440200916
|
|
|
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 |
rs762846821
|
|
|
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 |
rs121913529
|
|
|
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 |
rs1440200916
|
|
|
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 |
rs1057519803
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Oncogenic ERBB3 mutations in human cancers.
|
23680147 |
2013 |
rs36053993
|
|
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 |
rs36053993
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
MUTYH-associated colon disease: adenomatous polyposis is only one of the possible phenotypes. A family report and literature review.
|
22158503 |
2012 |
rs36053993
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
MUTYH mutations associated with familial adenomatous polyposis: functional characterization by a mammalian cell-based assay.
|
19953527 |
2010 |
rs36053993
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
MutYH mutation carriers have increased breast cancer risk.
|
21952991 |
2012 |
rs36053993
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
MUTYH gene expression and alternative splicing in controls and polyposis patients.
|
22473953 |
2012 |
rs36053993
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Loss of MUTYH function in human cells leads to accumulation of oxidative damage and genetic instability.
|
23108399 |
2013 |
rs36053993
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors.
|
11818965 |
2002 |
rs1452231640
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Importantly, L22P mice exhibit chronic inflammation accompanied by stomach tumors.
|
31412651 |
2019 |