Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7903146
rs7903146
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.020 GeneticVariation BEFREE Because the T allele of rs7903146 is common, if a causal link is established, this variant could account for a sizable proportion ( approximately 17% here) of cases of colon cancer in the general population. 18268068

2008

dbSNP: rs7903146
rs7903146
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.020 GeneticVariation BEFREE These data suggest that colon cancer risk associated with the rs7903146 TCF7L2 polymorphism is modified by use of aspirin/NSAIDs. 18398040

2008