Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587780345
rs587780345
T 0.700 CausalMutation CLINVAR

dbSNP: rs72559715
rs72559715
T 0.700 GeneticVariation CLINVAR

dbSNP: rs72559722
rs72559722
A 0.700 CausalMutation CLINVAR

dbSNP: rs72559734
rs72559734
T 0.700 CausalMutation CLINVAR

dbSNP: rs754729248
rs754729248
G 0.700 CausalMutation CLINVAR

dbSNP: rs76474829
rs76474829
G 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs769268803
rs769268803
T 0.700 CausalMutation CLINVAR

dbSNP: rs80356661
rs80356661
T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs948820149
rs948820149
C 0.700 GeneticVariation CLINVAR

dbSNP: rs12050217
rs12050217
0.010 GeneticVariation BEFREE <b>Conclusion</b>: For the first time, we showed that <i>BDKRB1</i> rs12050217 G allele is associated with protection for the advanced stage of DR in T2DM patients; however, further studies are needed to confirm this finding. 31017477

2019

dbSNP: rs13266634
rs13266634
1.000 GeneticVariation BEFREE <b>Conclusion:</b> The present meta-analysis demonstrated that <i>SLC30A8</i> rs13266634 was a potential risk factor for T2DM, and more studies should be performed to confirm the association between rs13266634 polymorphism and IGR. 30319545

2018

dbSNP: rs2230806
rs2230806
0.030 GeneticVariation BEFREE <b>Conclusion:</b> This study does not support the association between R219K polymorphism and T2DM-related MCI. 28824418

2017

dbSNP: rs7493
rs7493
0.020 GeneticVariation BEFREE <b>Conclusions:</b> The <i>PON2</i> Ser311Cys and Ala148Gly polymorphisms were not associated with the risk of developing T2DM in the Chinese population. 30210454

2018

dbSNP: rs12026
rs12026
0.020 GeneticVariation BEFREE <b>Conclusions:</b> The <i>PON2</i> Ser311Cys and Ala148Gly polymorphisms were not associated with the risk of developing T2DM in the Chinese population. 30210454

2018

dbSNP: rs11077
rs11077
0.010 GeneticVariation BEFREE <b>Methods:</b> We conducted a case-control study in genotyping of five polymorphic loci, including <i>RAN</i> rs14035, <i>XPO5</i> rs11077, <i>DICER1</i> rs13078, <i>DICER1</i> rs3742330, and <i>TARBP2</i> rs784567, in miRNA processing genes to explore the risk factors for T2DM and diabetic vascular complications. 31354628

2019

dbSNP: rs3742330
rs3742330
0.010 GeneticVariation BEFREE <b>Methods:</b> We conducted a case-control study in genotyping of five polymorphic loci, including <i>RAN</i> rs14035, <i>XPO5</i> rs11077, <i>DICER1</i> rs13078, <i>DICER1</i> rs3742330, and <i>TARBP2</i> rs784567, in miRNA processing genes to explore the risk factors for T2DM and diabetic vascular complications. 31354628

2019

dbSNP: rs784567
rs784567
0.010 GeneticVariation BEFREE <b>Methods:</b> We conducted a case-control study in genotyping of five polymorphic loci, including <i>RAN</i> rs14035, <i>XPO5</i> rs11077, <i>DICER1</i> rs13078, <i>DICER1</i> rs3742330, and <i>TARBP2</i> rs784567, in miRNA processing genes to explore the risk factors for T2DM and diabetic vascular complications. 31354628

2019

dbSNP: rs12050217
rs12050217
0.010 GeneticVariation BEFREE <b>Results</b>: The genotype frequencies of the <i>BDKRB1</i> rs12050217A/G polymorphism are in Hardy-Weinberg equilibrium and did not differ between T2DM patients and non-diabetic subjects (<i>P</i> > 0.05). 31017477

2019

dbSNP: rs1384565
rs1384565
0.010 GeneticVariation BEFREE <b>Results:</b> We found both rs1384565 CC genotype (12.1 compared with 6.6%, <i>P</i><0.001) and C allele (35.2 compared with 24.4%, <i>P</i><0.001) were more frequent in the T2DM patients than in the controls. 30413610

2018

dbSNP: rs2989924
rs2989924
0.010 GeneticVariation BEFREE <i>AQP7</i> SNP rs2989924 and rs3758269 were associated with T2DM risk in Chinese Han population. 30598999

2018

dbSNP: rs3758269
rs3758269
0.010 GeneticVariation BEFREE <i>AQP7</i> SNP rs2989924 and rs3758269 were associated with T2DM risk in Chinese Han population. 30598999

2018

dbSNP: rs6265
rs6265
0.030 GeneticVariation BEFREE <i>BDNF</i> gene Val66Met variation may be associated with cognitive deficits in T2DM, especially with delayed memory. 29423073

2018

dbSNP: rs759834365
rs759834365
0.020 GeneticVariation BEFREE <i>BDNF</i> gene Val66Met variation may be associated with cognitive deficits in T2DM, especially with delayed memory. 29423073

2018

dbSNP: rs4778889
rs4778889
0.010 GeneticVariation BEFREE <i>IL-16</i> rs4778889 polymorphism showed no significant association with T2DM risk.<b>Conclusion:</b><i>IL-16</i> gene rs11556218 polymorphism was significantly associated with T2DM susceptibility in the Chinese Han population, while rs4778889 was not. 31375554

2019

dbSNP: rs3752462
rs3752462
0.010 GeneticVariation BEFREE <i>MYH9</i> rs3752462 (T>C) and <i>APOL1</i> rs136161 (C>G) were genotyped in 303 DKD patients and 364 type 2 diabetes mellitus (T2DM) patients without kidney disease using the TaqMan SNP genotyping assay. 29862302

2018