rs5522, NR3C2

N. diseases: 19
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Depressed mood
CUI: C0344315
Disease: Depressed mood
0.050 GeneticVariation BEFREE To investigate the hypothesis that the MR sex-dependently influences the relation between childhood maltreatment and depression, we investigated three common and functional MR haplotypes (GA, CA, and CG haplotype, based on rs5522 and rs2070951) in a population-based cohort (N = 665) and an independent clinical cohort from the Netherlands Study of Depression and Anxiety (NESDA) (N = 1639). 25686805 2015
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
0.050 GeneticVariation BEFREE To investigate the hypothesis that the MR sex-dependently influences the relation between childhood maltreatment and depression, we investigated three common and functional MR haplotypes (GA, CA, and CG haplotype, based on rs5522 and rs2070951) in a population-based cohort (N = 665) and an independent clinical cohort from the Netherlands Study of Depression and Anxiety (NESDA) (N = 1639). 25686805 2015
Mental Depression
CUI: C0011570
Disease: Mental Depression
0.050 GeneticVariation BEFREE To investigate the hypothesis that the MR sex-dependently influences the relation between childhood maltreatment and depression, we investigated three common and functional MR haplotypes (GA, CA, and CG haplotype, based on rs5522 and rs2070951) in a population-based cohort (N = 665) and an independent clinical cohort from the Netherlands Study of Depression and Anxiety (NESDA) (N = 1639). 25686805 2015
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
0.050 GeneticVariation BEFREE There is evidence that the Val allele of the MRI180V polymorphism (rs5522) increases the risk of depression, attention and cognitive deficits. 22584804 2013
Mental Depression
CUI: C0011570
Disease: Mental Depression
0.050 GeneticVariation BEFREE There is evidence that the Val allele of the MRI180V polymorphism (rs5522) increases the risk of depression, attention and cognitive deficits. 22584804 2013
Depressed mood
CUI: C0344315
Disease: Depressed mood
0.050 GeneticVariation BEFREE There is evidence that the Val allele of the MRI180V polymorphism (rs5522) increases the risk of depression, attention and cognitive deficits. 22584804 2013
Mental Depression
CUI: C0011570
Disease: Mental Depression
0.050 GeneticVariation BEFREE Common functional MR single nucleotide polymorphisms (SNPs; MR -2G/C and I180V) and haplotypes were tested for association with variability in the CAR in a large cohort (Netherlands Study of Depression and Anxiety, NESDA) of patients diagnosed with a lifetime major depressive disorder (MDD). 20884124 2011
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
0.050 GeneticVariation BEFREE In an elderly cohort, one of the functional MR gene variants, MR-I180V, associated with higher feelings of depression. 21164267 2011
Depressed mood
CUI: C0344315
Disease: Depressed mood
0.050 GeneticVariation BEFREE In an elderly cohort, one of the functional MR gene variants, MR-I180V, associated with higher feelings of depression. 21164267 2011
Depressed mood
CUI: C0344315
Disease: Depressed mood
0.050 GeneticVariation BEFREE Common functional MR single nucleotide polymorphisms (SNPs; MR -2G/C and I180V) and haplotypes were tested for association with variability in the CAR in a large cohort (Netherlands Study of Depression and Anxiety, NESDA) of patients diagnosed with a lifetime major depressive disorder (MDD). 20884124 2011
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
0.050 GeneticVariation BEFREE Common functional MR single nucleotide polymorphisms (SNPs; MR -2G/C and I180V) and haplotypes were tested for association with variability in the CAR in a large cohort (Netherlands Study of Depression and Anxiety, NESDA) of patients diagnosed with a lifetime major depressive disorder (MDD). 20884124 2011
Mental Depression
CUI: C0011570
Disease: Mental Depression
0.050 GeneticVariation BEFREE In an elderly cohort, one of the functional MR gene variants, MR-I180V, associated with higher feelings of depression. 21164267 2011
Mental Depression
CUI: C0011570
Disease: Mental Depression
0.050 GeneticVariation BEFREE Future studies are warranted to evaluate whether rs5522 genotype interacts with naturalistic stressors to increase the risk of depression and whether stress-induced anhedonia might moderate such risk. 20528958 2010
Depressed mood
CUI: C0344315
Disease: Depressed mood
0.050 GeneticVariation BEFREE Future studies are warranted to evaluate whether rs5522 genotype interacts with naturalistic stressors to increase the risk of depression and whether stress-induced anhedonia might moderate such risk. 20528958 2010
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
0.050 GeneticVariation BEFREE Future studies are warranted to evaluate whether rs5522 genotype interacts with naturalistic stressors to increase the risk of depression and whether stress-induced anhedonia might moderate such risk. 20528958 2010
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.030 GeneticVariation BEFREE Genetic variation in <i>MR</i> (rs5522) and comorbidity with hypertension were significantly and potentially associated with prognosis when treated with ADT, respectively. 30619769 2018
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.030 GeneticVariation BEFREE The aim of this study was to analyze the association between the MR p.I180V polymorphism with hypertension and markers of cardiovascular risk. 19955850 2010
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
0.030 GeneticVariation BEFREE One haplotype, which included the G allele of the rs5522</span>, was also associated with reduced risk of HTN and four haplotypes which included the A allele were associated with increased risk of HTN. 19325532 2009
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
0.020 GeneticVariation BEFREE Previous research found that variants of the glucocorticoid receptor (GR) (9β, ER22/23EK, BclI, TthIIIl, NR3C1-1 and N363S) and mineralocorticoid receptor (MR) gene polymorphism (-2 C/G and I180V) are associated with both glucocorticoid (GC) sensitivity and major depressive disorder (MDD). 25765757 2015
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
0.020 GeneticVariation BEFREE Common functional MR single nucleotide polymorphisms (SNPs; MR -2G/C and I180V) and haplotypes were tested for association with variability in the CAR in a large cohort (Netherlands Study of Depression and Anxiety, NESDA) of patients diagnosed with a lifetime major depressive disorder (MDD). 20884124 2011
High altitude pulmonary edema
CUI: C0340100
Disease: High altitude pulmonary edema
0.010 GeneticVariation BEFREE The rs5522 polymorphism of the NR3C2 gene was associated with HAPE </span>susceptibility in Chinese subjects. 30292562 2018
Chronic central serous chorioretinopathy
0.010 GeneticVariation BEFREE Moreover, the GA haplotype of single-nucleotide polymorphisms rs2070951 and rs5522 in NR3C2 conferred risk for cCSC (odds ratio, 1.39; 95% CI, 1.15-1.68; P = .004), whereas the CA haplotype decreased risk for cCSC (odds ratio, 0.72; 95% CI, 0.60-0.87; P < .001). 28334414 2017
Left Ventricular Hypertrophy
CUI: C0149721
Disease: Left Ventricular Hypertrophy
0.010 GeneticVariation BEFREE Left ventricular hypertrophy (LVH) was more prevalent in G carriers than AA homozygous for rs5522 but not for rs2070951 in RHTN. 26049084 2016
Resistant hypertensive disorder
CUI: C0745130
Disease: Resistant hypertensive disorder
0.010 GeneticVariation BEFREE Association of Mineralocorticoid Receptor Polymorphism I180V With Left Ventricular Hypertrophy in Resistant Hypertension. 26049084 2016
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
0.010 GeneticVariation BEFREE Interaction between GR and MR polymorphisms and antenatal glucocorticoid treatment was observed, with poorer IQ scores for exposed N363S carriers; poorer intellectual subdomain scores for exposed I180V-carriers; more favorable total problem behavior scores for exposed R23K carriers. 25406795 2015