Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913529
rs121913529
KRAS
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.710 CausalMutation CLINVAR

dbSNP: rs104886003
rs104886003
PIK3CA
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519044
rs1057519044
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519803
rs1057519803
ERBB3
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		A 0.700 GeneticVariation CLINVAR Oncogenic ERBB3 mutations in human cancers. 23680147

2013
dbSNP: rs1057519836
rs1057519836
CTNNB1
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		G 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121434595
rs121434595
NRAS
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121908382
rs121908382
MUTYH
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		A 0.700 CausalMutation CLINVAR

dbSNP: rs121908383
rs121908383
MUTYH
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		C 0.700 CausalMutation CLINVAR

dbSNP: rs121909144
rs121909144
KLF6
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR

dbSNP: rs121909775
rs121909775
CASP10
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR

dbSNP: rs121909776
rs121909776
CASP10
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		C 0.700 CausalMutation CLINVAR

dbSNP: rs121912469
rs121912469
IRF1
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		A 0.700 CausalMutation CLINVAR

dbSNP: rs121913228
rs121913228
CTNNB1
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		C 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913279
rs121913279
PIK3CA
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		G 0.700 CausalMutation CLINVAR

dbSNP: rs121913281
rs121913281
PIK3CA
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR

dbSNP: rs121913403
rs121913403
CTNNB1
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		A 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014
dbSNP: rs121913478
rs121913478
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		C 0.700 CausalMutation CLINVAR

dbSNP: rs121913530
rs121913530
KRAS
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR

dbSNP: rs121918487
rs121918487
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR

dbSNP: rs121918491
rs121918491
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR

dbSNP: rs121918505
rs121918505
FGFR2
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		G 0.700 CausalMutation CLINVAR

dbSNP: rs137854571
rs137854571
APC
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR

dbSNP: rs137854573
rs137854573
APC
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR

dbSNP: rs137854575
rs137854575
APC
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		A 0.700 CausalMutation CLINVAR

dbSNP: rs140342925
rs140342925
MUTYH
CUI: C0038356
Disease: Stomach Neoplasms
Stomach Neoplasms 		T 0.700 CausalMutation CLINVAR