Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913529
rs121913529
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.710 GeneticVariation UNIPROT BRAF and KRAS mutations in stomach cancer. 14534542

2003

dbSNP: rs121913529
rs121913529
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: rs121913529
rs121913529
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: rs104894361
rs104894361
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT BRAF and KRAS mutations in stomach cancer. 14534542

2003

dbSNP: rs104894361
rs104894361
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
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: rs112445441
rs112445441
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT

dbSNP: rs1203145163
rs1203145163
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT

dbSNP: rs121908382
rs121908382
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT Functional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain. 25820570

2015

dbSNP: rs121908382
rs121908382
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT Tumor markers in colorectal cancer, gastric cancer and gastrointestinal stromal cancers: European group on tumor markers 2014 guidelines update. 23852704

2014

dbSNP: rs121908382
rs121908382
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT Genetic alterations of the MYH gene in gastric cancer. 15273732

2004

dbSNP: rs121908383
rs121908383
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT Functional Complementation Assay for 47 MUTYH Variants in a MutY-Disrupted Escherichia coli Strain. 25820570

2015

dbSNP: rs121908383
rs121908383
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT Tumor markers in colorectal cancer, gastric cancer and gastrointestinal stromal cancers: European group on tumor markers 2014 guidelines update. 23852704

2014

dbSNP: rs121908383
rs121908383
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT Genetic alterations of the MYH gene in gastric cancer. 15273732

2004

dbSNP: rs121909776
rs121909776
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT Tumor markers in colorectal cancer, gastric cancer and gastrointestinal stromal cancers: European group on tumor markers 2014 guidelines update. 23852704

2014

dbSNP: rs121909776
rs121909776
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT Inactivating mutations of the caspase-10 gene in gastric cancer. 11973654

2002

dbSNP: rs121912469
rs121912469
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT Tumor markers in colorectal cancer, gastric cancer and gastrointestinal stromal cancers: European group on tumor markers 2014 guidelines update. 23852704

2014

dbSNP: rs121912469
rs121912469
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
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
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: rs121912470
rs121912470
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: rs121913528
rs121913528
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT BRAF and KRAS mutations in stomach cancer. 14534542

2003

dbSNP: rs121913528
rs121913528
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
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: rs121913530
rs121913530
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.700 GeneticVariation UNIPROT BRAF and KRAS mutations in stomach cancer. 14534542

2003