Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7903146
rs7903146
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE A similar relation was observed for the genotype T/T of the rs7903146 polymorphism and the rectal location of cancer (OR=7.57, P=0.0403). 27755946 2016
dbSNP: rs7903146
rs7903146
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE The allele (P = 0.033) frequency of rs7903146 (T) polymorphism was significantly higher in the cancer patients than normal individuals. 21301999 2012
dbSNP: rs290481
rs290481
Entrez Id: 6934
Gene Symbol: TCF7L2
TCF7L2
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE T2D-related variants HHEX rs7923837, TCF7L2 rs290481 and CDKAL1 rs7756992 increased cancer risk in patients with diabetes. 24468095 2014