Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7903146
rs7903146
TCF7L2
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		0.030 GeneticVariation BEFREE The strong LD existed between the 2 single nucleotide polymorphisms and haplotype T-T (rs7903146-rs290487) increased the susceptibility to DN (OR = 2.63, 95% CI = 1.31-5.25).TCF7L2 rs7903146 polymorphism may be associated with the susceptibility to DN in Chinese Han population, but rs290487 is not. 30290587

2018
dbSNP: rs7903146
rs7903146
TCF7L2
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		0.030 GeneticVariation BEFREE Analysis of TCF7L2 rs7903146 in normal controls and diabetics with or without nephropathy demonstrated that the 'T' allele is associated with both diabetes (p = 0.049) and DN (p = 0.024), but this association is not independent of T2DM. 25185853

2014
dbSNP: rs7903146
rs7903146
TCF7L2
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		0.030 GeneticVariation BEFREE In our study the T allele of the rs7903146 SNP in the TCF7L2 gene confers the risk of developing diabetic nephropathy. 24574000

2014