Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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