rs12523822
|
|
|
0.710 |
GeneticVariation |
BEFREE |
Within ethnic group meta-analysis of discovery GWAS and replication set results identified genome-wide significant evidence for association between DKD and rs12523822 on chromosome 6q25.2 in American Indians (P = 5.74x10-9).
|
26305897 |
2015 |
rs955333
|
|
|
0.710 |
GeneticVariation |
BEFREE |
<i>Background</i>.Genome-wide association studies found rs955333 located in 6q25.2 was associated with diabetic kidney disease in multiple ethnic populations, including European Americans, African Americans, and Mexican Americans.
|
28401168 |
2017 |
rs9942471
|
|
|
0.710 |
GeneticVariation |
BEFREE |
Analysis of specific DKD phenotypes identified a novel signal near <i>GABRR1</i> (rs9942471, <i>P</i> = 4.5 × 10<sup>-8</sup>) associated with microalbuminuria in European T2D case subjects.
|
29703844 |
2018 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
This case-control study assessed the association of MTHFR C677T mutation in T2DM and DN cases.
|
21186995 |
2011 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The methylenetetrahydrofolate reductase 677 C/T genotypes were determined in 174 type 2 diabetic patients: 80 with and 94 without renal failure due to diabetic nephropathy.
|
12784186 |
2003 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Our study for the first time demonstrated a synergistic effect between ACE I/D with either MTHFR C677T or A1298C polymorphism on the increased risk of DN among patients with T2DM.
|
21942443 |
2012 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Effects of the C677T and A1298C polymorphisms of the MTHFR gene on the genetic predisposition for diabetic nephropathy.
|
12897091 |
2003 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Here, we first adopted methylenetetrahytrofolate reductase (MTHFR) gene C677T polymorphism as an instrument to infer the possible causal relevance between circulating homocysteine and DKD risk in a Chinese population and next attempted to build a risk prediction model for DKD.
|
30729677 |
2019 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
C677T polymorphism in MTHFR gene may be a risk factor for DN, but not for DM, in a Chinese population.
|
22209973 |
2012 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The current meta-analysis suggested that MTHFR C677T polymorphism might influence DN risk, but not for DM in the Chinese population.
|
23822721 |
2013 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Our findings suggest that the C677T mutation in the MTHFR gene predisposes type 2 diabetes patients to the development of diabetic nephropathy.
|
14737040 |
2004 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The contribution of C677T single nucleotide polymorphism to increased risk of DN (presumably by increasing homocysteine concentrations) must be evaluated in the context of the ethnic background.
|
20524928 |
2010 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The present study has investigated the role of endothelial nitric oxide (eNOS) G894T polymorphism and its interaction with methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C variants on the predisposition to diabetic nephropathy and its progression.
|
21380725 |
2011 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
In conclusion, although there is some evidence of association between MTHFR C677T gene polymorphism and DN, the above findings reinforce the need for further and more rigorous association studies.
|
17805475 |
2007 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Interaction of MTHFR C677T polymorphism with smoking in susceptibility to diabetic nephropathy in Chinese men with type 2 diabetes.
|
30397262 |
2019 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
MTHFR C677T and A1298C gene polymorphisms and hyperhomocysteinemia as risk factors of diabetic nephropathy in type 2 diabetes patients.
|
16828193 |
2007 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
We observed a significant association of MTHFR C677T with development of diabetic nephropathy in type 2 diabetics.
|
23846111 |
2013 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Folate supplementation in diabetic patients with the C677T mutation and low-normal serum folate may prevent the onset or retard the progression of DN.
|
11015479 |
2000 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
This meta-analysis showed that the MTHFR C677T variants may influence DN risk in Chinese, and further studies with gene-gene and gene-environment interactions are required for definite conclusions.
|
26072975 |
2016 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
MTHFR C677T gene polymorphism associated with a predisposition to increased plasma homocysteine levels may represent a genetic risk factor for diabetic nephropathy in Chinese type 2 diabetic patients.
|
15126006 |
2004 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
These findings suggest that the C677T and A1298C polymorphism of MTHFR gene was associated with diabetic nephropathy in a south Indian population.
|
29227003 |
2019 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
To find whether polymorphisms of methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C are risk factors for diabetic nephropathy (DN) among type 2 diabetes mellitus (T2DM) patients from Western Iran.
|
20800057 |
2010 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
An updated meta-analysis of methylenetetrahydrofolate reductase gene 677C/T polymorphism with diabetic nephropathy and diabetic retinopathy.
|
22056717 |
2012 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Using both a large case-control and a follow-up study, we found no evidence that the C677T MTHFR polymorphism has a significant role in the development of diabetic nephropathy in type 1 diabetes.
|
12776270 |
2003 |
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
There was a significant correlation of plasma homocysteine level with microalbuminuria (r = 0.54; P = 0.031) in the patients with diabetic nephropathy who had C677T polymorphism.
|
19598005 |
2009 |