Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs746481984
rs746481984
CDH1
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		G 0.720 CausalMutation CLINVAR

dbSNP: rs587780537
rs587780537
CDH1
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs555607708
rs555607708
CHEK2
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		A 0.700 CausalMutation CLINVAR

dbSNP: rs372481703
rs372481703
APC
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs367807476
rs367807476
STK11
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs202208566
rs202208566
TCHP
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs180177133
rs180177133
PALB2
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1555515731
rs1555515731
CDH1
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1400295986
rs1400295986
APC
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs1203145163
rs1203145163
TFF1 ; LOC105372815
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs112445441
rs112445441
KRAS
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT

dbSNP: rs121913529
rs121913529
KRAS
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.710 GeneticVariation UNIPROT Activated c-Ha-ras oncogene with a guanine to thymine transversion at the twelfth codon in a human stomach cancer cell line. 3034404

1987
dbSNP: rs121913530
rs121913530
KRAS
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT Activated c-Ha-ras oncogene with a guanine to thymine transversion at the twelfth codon in a human stomach cancer cell line. 3034404

1987
dbSNP: rs121913528
rs121913528
KRAS
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT Activated c-Ha-ras oncogene with a guanine to thymine transversion at the twelfth codon in a human stomach cancer cell line. 3034404

1987
dbSNP: rs104894361
rs104894361
KRAS
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT Activated c-Ha-ras oncogene with a guanine to thymine transversion at the twelfth codon in a human stomach cancer cell line. 3034404

1987
dbSNP: rs121913529
rs121913529
KRAS
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.710 GeneticVariation UNIPROT Clinicopathologic significance of the K-ras gene codon 12 point mutation in stomach cancer. An analysis of 140 cases. 7773929

1995
dbSNP: rs121913530
rs121913530
KRAS
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT Clinicopathologic significance of the K-ras gene codon 12 point mutation in stomach cancer. An analysis of 140 cases. 7773929

1995
dbSNP: rs121913528
rs121913528
KRAS
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT Clinicopathologic significance of the K-ras gene codon 12 point mutation in stomach cancer. An analysis of 140 cases. 7773929

1995
dbSNP: rs104894361
rs104894361
KRAS
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT Clinicopathologic significance of the K-ras gene codon 12 point mutation in stomach cancer. An analysis of 140 cases. 7773929

1995
dbSNP: rs121912470
rs121912470
IRF1
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT Functionally inactivating point mutation in the tumor-suppressor IRF-1 gene identified in human gastric cancer. 9679752

1998
dbSNP: rs121912469
rs121912469
IRF1
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT Functionally inactivating point mutation in the tumor-suppressor IRF-1 gene identified in human gastric cancer. 9679752

1998
dbSNP: rs121912470
rs121912470
IRF1
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT Interferon regulatory factor 1 tryptophan 11 to arginine point mutation abolishes DNA binding. 10395927

1999
dbSNP: rs121912469
rs121912469
IRF1
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.700 GeneticVariation UNIPROT Interferon regulatory factor 1 tryptophan 11 to arginine point mutation abolishes DNA binding. 10395927

1999
dbSNP: rs1052133
rs1052133
OGG1 ; CAMK1
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.100 GeneticVariation BEFREE We examined the distribution of the hOGG1 Ser326Cys polymorphism and its presumed correlation with gastric cancer risk in two case-control studies of different ethnic groups in São Paulo, Brazil. 11448535

2001
dbSNP: rs35187787
rs35187787
CDH1
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 GeneticVariation BEFREE However, the fact that this alteration (Ala592Thr) segregated with colon cancer and diffuse gastric cancer in one big family, suggests that this E-cadherin missense alteration, beside predisposing to diffuse gastric cancer, also may play a role in colorectal carcinogenesis. 11562785

2001