Varaico: Literature-Extracted Genetic Variants

Gene:NR3C1
Variant:p.G103E
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NR3C1

NM_000176.3:p.G103E

Associated Papers

TNF-α -1031T/C and -863C/A polymorphisms are associated with dyslipidaemia.

Lin K et al.

The British Journal of Nutrition, 2025

Host genetic variants in sepsis risk: a field synopsis and meta-analysis.

Lu H et al.

Critical Care (london, England), 2019

30683156 (PubMed )
Supplement: 13054_2019_2313_MOESM1_ESM.docx

TNF-α and IL-1 β Cytokine Gene Polymorphism in Patients with Nasal Polyposis.

İsmi O et al.

Turkish Archives of Otorhinolaryngology, 2017

Glucocorticoid Receptor Gene Variants and Neonatal Outcome in Very-Low-Birth-Weight Preterm Infants.

Schreiner C et al.

Neonatology, 2017

Pharmacogenetic considerations for acute lymphoblastic leukemia therapies.

Dulucq S et al.

Expert Opinion on Drug Metabolism & Toxicology, 2014

Assessment of 11-β hydroxysteroid dehydrogenase (11-βHSD1) 4478T>G and tumor necrosis factor-α (TNF-α)-308G>A polymorphisms with obesity and insulin resistance in Asian Indians in North India.

Sharma M et al.

Molecular Biology Reports, 2013

Association between tumor necrosis factor-α promoter -308 A/G, -238 A/G, interleukin-6 -174 G/C and -572 G/C polymorphisms and periodontal disease: a meta-analysis.

Song GG et al.

Molecular Biology Reports, 2013

Analysis of COCH and TNFA variants in East Indian primary open-angle glaucoma patients.

Chakraborty S et al.

Biomed Research International, 2013

Association of IL1A, IL1B, ILRN, IL6, IL10 and TNF-α polymorphisms with risk and clinical course of multiple sclerosis in a Polish population.

Mirowska-Guzel D et al.

Journal of Neuroimmunology, 2011

Poor replication of candidate genes for major depressive disorder using genome-wide association data.

Bosker FJ et al.

Molecular Psychiatry, 2011

IL-10 and TNF-alpha promoter haplotypes are associated with childhood Crohn's disease location.

Sanchez R et al.

World Journal of Gastroenterology, 2009

The molecular-genetic basis of functional hyperandrogenism and the polycystic ovary syndrome.

Escobar-Morreale HF et al.

Endocrine Reviews, 2005

A common functional polymorphism (C-->A substitution at position -863) in the promoter region of the tumour necrosis factor-alpha (TNF-alpha) gene associated with reduced circulating levels of TNF-alpha.

Skoog T et al.

Human Molecular Genetics, 1999

Gene polymorphism association studies in dialysis: the nutrition-inflammation axis.

Stenvinkel P et al.

Seminars in Dialysis, 0

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