Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104886003
rs104886003
PIK3CA
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519044
rs1057519044
FGFR2
T 0.700 GeneticVariation CLINVAR

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

2013
dbSNP: rs1057519836
rs1057519836
CTNNB1
G 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
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: rs121434595
rs121434595
NRAS
T 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121908382
rs121908382
MUTYH
A 0.700 CausalMutation CLINVAR

dbSNP: rs121908383
rs121908383
MUTYH
C 0.700 CausalMutation CLINVAR

dbSNP: rs121909144
rs121909144
KLF6
T 0.700 CausalMutation CLINVAR

dbSNP: rs121909775
rs121909775
CASP10
T 0.700 CausalMutation CLINVAR

dbSNP: rs121909776
rs121909776
CASP10
C 0.700 CausalMutation CLINVAR

dbSNP: rs121912469
rs121912469
IRF1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121913228
rs121913228
CTNNB1
C 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913279
rs121913279
PIK3CA
G 0.700 CausalMutation CLINVAR

dbSNP: rs121913281
rs121913281
PIK3CA
T 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: rs121913478
rs121913478
FGFR2
C 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: rs121918487
rs121918487
FGFR2
T 0.700 CausalMutation CLINVAR

dbSNP: rs121918491
rs121918491
FGFR2
T 0.700 CausalMutation CLINVAR

dbSNP: rs121918505
rs121918505
FGFR2
G 0.700 CausalMutation CLINVAR

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