Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3758391
rs3758391
0.030 GeneticVariation BEFREE The polymorphisms rs3758391 and rs1800470 located in SIRT1 and TGF-β1 have been associated with type 2 diabetes in different populations but its functional effect is not clear. 31799723

2020

dbSNP: rs7896005
rs7896005
0.030 GeneticVariation BEFREE Multivariate model analysis, including T2D status, age, and body mass index (BMI), displayed significant covariance in PPARGC-1α rs8192678; SIRT1 rs7896005; TCF7L2 rs7903146 and rs122243326; UCP3 rs3781907; and HHEX rs1111875 with a P < 0.05. 31759989

2020

dbSNP: rs3758391
rs3758391
0.030 GeneticVariation BEFREE We failed to find any significant association between rs3758391 polymorphisms and T2DM, DF susceptibility. 29995800

2018

dbSNP: rs7896005
rs7896005
0.030 GeneticVariation BEFREE All polymorphisms were in Hardy-Weinberg equilibrium, and the association by genotype with T2D-related traits displayed nominal significance for rs8192678 with glucose (<i>p</i> = 0.023) and triglycerides (<i>p</i> = 0.013); rs2010963 with diastolic blood pressure (DBP) (<i>p</i> = 0.012) and cholesterol (<i>p</i> = 0.013); rs7896005 with DBP (<i>p</i> = 0.012) and insulin (<i>p</i> = 0.011); and rs659366 with cholesterol (<i>p</i> = 0.034), glucose (<i>p</i> = 0.031) and triglycerides (<i>p</i> = 0.028); and the association of rs2010963 with HDL-C (<i>p</i> = 0.0007) was significant. 30393491

2018

dbSNP: rs7896005
rs7896005
0.030 GeneticVariation BEFREE Two tag SNPs, rs10509291 and rs7896005, were nominally associated with type 2 diabetes (P=0.01, OR=1.25 95%CI 1.05-1.48, and P=0.02, OR=1.17 95%CI 1.02-1.34, respectively; additive P values adjusted for age, sex, birth year, and family membership), but not BMI (adjusted P values 0.52 and 0.45, respectively). 21871827

2011

dbSNP: rs3758391
rs3758391
0.030 GeneticVariation BEFREE Nominally significant associations were also observed between T2D and the SIRT1 rs3758391 SNP and MS and the HHEX rs5015480 polymorphism. 20503258

2010

dbSNP: rs12778366
rs12778366
0.010 GeneticVariation BEFREE The results were adjusted using logistic regression analysis.C allele of rs12778366 polymorphism was significantly correlated with reduced DF susceptibility which deriving from healthy controls (adjusted OR = 0.364, 95% CI = 0.158-0.835) so was patients with T2DM (P = .047, OR = 0.591, 95%CI = 0.349-0.998), but the results became nonsignificant adjusted by clinical features (adjusted OR = 0.654, 95% CI = 0.391-1.094). 29995800

2018

dbSNP: rs4746720
rs4746720
0.010 GeneticVariation BEFREE Variants in <i>SIRT1</i> with rs4746720 CC+TT genotype increased the risk of T2DM, especially with the unhealthy eating habits. 30320001

2018

dbSNP: rs10823108
rs10823108
0.010 GeneticVariation BEFREE In conclusion, genetic variant rs10823108 in SIRT1 and variant rs17446614 in FoxO1 may contribute to the risk of DN in T2DM patients. 28860538

2017

dbSNP: rs1467568
rs1467568
0.010 GeneticVariation BEFREE Minor alleles of these SNPs were associated with a lower prevalence of type 2 diabetes only in individuals who had been exposed to famine prenatally (odds ratio for rs7895833 0.50 [95% CI 0.24-1.03], P = 0.06; for rs1467568 0.48 [0.25-0.91], P = 0.02). 22228742

2012