Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Diabetes Mellitus, Non-Insulin-Dependent
0.730 GeneticVariation BEFREE Our findings are consistent with a true association between rs</span>10911021 and CHD in T2D. 27549350 2016
Diabetes Mellitus, Non-Insulin-Dependent
0.730 GeneticVariation BEFREE These results extend the association of GLUL rs10911021 to incident CVD morbidity and mortality in the setting of T2D. 26395743 2016
Diabetes Mellitus, Non-Insulin-Dependent
0.730 GeneticVariation BEFREE These findings point to SNP rs10911021 as an independent modulator of mortality in patients with type 2 diabetes and, together with the previous observation, suggest that this results from an effect of this variant on cardiovascular risk. 25677913 2015
Diabetes Mellitus, Non-Insulin-Dependent
0.730 GeneticVariation GWASCAT Association between a genetic variant related to glutamic acid metabolism and coronary heart disease in individuals with type 2 diabetes. 23982368 2013
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.710 GeneticVariation BEFREE Over a median of 9.6 years of follow-up, the risk (C) allele for GLUL r</span>s10911021 was significantly associated with the primary composite end point of death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for angina among individuals with no history of cardiovascular disease (CVD) at baseline using additive genetic models (hazard ratio 1.17 [95% CI 1.01-1.36]; P = 0.032). 26395743 2016
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.710 GeneticVariation GWASCAT Association between a genetic variant related to glutamic acid metabolism and coronary heart disease in individuals with type 2 diabetes. 23982368 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.040 GeneticVariation BEFREE The SNP rs10911021 was associated with CHD only in patients having diabetes, but the SNP was associated with total oxidative stress biomarkers MDA and GSH and GSSG levels. 29304826 2018
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.040 GeneticVariation BEFREE Our findings are consistent with a true association between rs</span>10911021</span> and CHD in T2D. 27549350 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.040 GeneticVariation BEFREE Single nucleotide polymorphism (SNP) rs10911021 at the glutamate-ammonia ligase (GLUL) locus has been associated with an increased risk of coronary heart disease in individuals with type 2 diabetes. 25677913 2015
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.040 GeneticVariation BEFREE A single-nucleotide polymorphism (rs10911021) was identified that was significantly associated with CHD among persons with diabetes but not in those without diabetes and was functionally related to glutamic acid metabolism, suggesting a mechanistic link. 23982368 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.020 GeneticVariation BEFREE The SNP rs10911021 is associated with oxidative stress in coronary heart disease patients from Pakistan. 29304826 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.020 GeneticVariation BEFREE The SNP rs10911021 was associated with CHD only in patients having diabetes, but the SNP was associated with total oxidative stress biomarkers MDA and GSH and GSSG levels. 29304826 2018
Diabetes
CUI: C0011847
Disease: Diabetes
0.020 GeneticVariation BEFREE The SNP rs10911021 was associated with CHD only in patients having diabetes, but the SNP was associated with total oxidative stress biomarkers MDA and GSH and GSSG levels. 29304826 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.020 GeneticVariation BEFREE The SNP rs10911021 is associated with oxidative stress in coronary heart disease patients from Pakistan. 29304826 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
0.020 GeneticVariation BEFREE Single nucleotide polymorphism (SNP) rs10911021 at the glutamate-ammonia ligase (GLUL) locus has been associated with an increased risk of coronary heart disease in individuals with type 2 diabetes. 25677913 2015
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.020 GeneticVariation BEFREE Single nucleotide polymorphism (SNP) rs10911021 at the glutamate-ammonia ligase (GLUL) locus has been associated with an increased risk of coronary heart disease in individuals with type 2 diabetes. 25677913 2015
Diabetes
CUI: C0011847
Disease: Diabetes
0.020 GeneticVariation BEFREE A single-nucleotide polymorphism (rs10911021) was identified that was significantly associated with CHD among persons with diabetes but not in those without diabetes and was functionally related to glutamic acid metabolism, suggesting a mechanistic link. 23982368 2013
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
0.020 GeneticVariation BEFREE A single-nucleotide polymorphism (rs10911021) was identified that was significantly associated with CHD among persons with diabetes but not in those without diabetes and was functionally related to glutamic acid metabolism, suggesting a mechanistic link. 23982368 2013
Heart Diseases
CUI: C0018799
Disease: Heart Diseases
0.010 GeneticVariation BEFREE As the SNP rs10911021 showed significant association with oxidative stress parameters and these parameters should an increased oxidative stress in the CHD subjects, it can be concluded that the SNP may have contributed to increase the risk of heart diseases in the diabetic subjects by increasing the oxidative stress. 29304826 2018
Obesity
CUI: C0028754
Disease: Obesity
0.010 GeneticVariation BEFREE We sought to determine whether GLUL rs10911021 is associated prospectively with adjudicated cardiovascular composite end points among overweight/obese individuals with T2D and whether a lifestyle intervention resulting in weight loss could diminish this association. 26395743 2016
Angina Pectoris
CUI: C0002962
Disease: Angina Pectoris
0.010 GeneticVariation BEFREE Over a median of 9.6 years of follow-up, the risk (C) allele for GLUL rs10911021 was significantly associated with the primary composite end point of death from cardiovascular causes, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for angina among individuals with no history of cardiovascular disease (CVD) at baseline using additive genetic models (hazard ratio 1.17 [95% CI 1.01-1.36]; P = 0.032). 26395743 2016
Cardiovascular morbidity
CUI: C1301700
Disease: Cardiovascular morbidity
0.010 GeneticVariation BEFREE Prospective Association of GLUL rs10911021 With Cardiovascular Morbidity and Mortality Among Individuals With Type 2 Diabetes: The Look AHEAD Study. 26395743 2016