Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800795
rs1800795
CUI: C0018133
Disease: Graft-vs-Host Disease
Graft-vs-Host Disease
0.010 GeneticVariation BEFREE Furthermore, the IL-6R rs4845618 donor genotype showed an association with severe acute graft-versus-host disease (GVHD), whereas the donor genotype of the IL-6 SNP rs1800795 was associated with decreased survival 100 days post-transplant. 29513361

2018

dbSNP: rs1800795
rs1800795
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis
0.010 GeneticVariation BEFREE GG genotypes of rs1800795 in IL-6 was also associated with occurrence of tuberculosis in our patients with TA. 28438554

2018

dbSNP: rs1800795
rs1800795
CUI: C0220630
Disease: Adult Liver Carcinoma
Adult Liver Carcinoma
0.010 GeneticVariation BEFREE Subgroup analyses of rs1800797 also suggested non-significant association and rs1800795 played a protective role in liver cancer. 29842912

2018

dbSNP: rs1800795
rs1800795
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease
0.010 GeneticVariation BEFREE The study was conducted to investigate the association of CRP rs1130864 (1444C/T), IL-6 rs1800795 (-174G/C) and LEPR rs1137101 (Q223R) genes with OSA and NAFLD in Asian Indians residing in North India. 30001365

2018

dbSNP: rs1800795
rs1800795
Congenital arteriovenous malformation
0.010 GeneticVariation BEFREE We genotyped 11 candidate variants: four variants reported as associated with lung AVM in HHT (PTPN14 rs2936018, USH2A rs700024, ADAM17 rs12474540, rs10495565), and seven variants reported as associated with sporadic BAVM or ICH (APOE ε2, ANGPTL4 rs11672433, EPHB4 rs314308, IL6 rs1800795, IL1B rs1143627, ITGB8 rs10486391, TNFA rs361525). 29932521

2018

dbSNP: rs1800795
rs1800795
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive
0.010 GeneticVariation BEFREE The study was conducted to investigate the association of CRP rs1130864 (1444C/T), IL-6 rs1800795 (-174G/C) and LEPR rs1137101 (Q223R) genes with OSA and NAFLD in Asian Indians residing in North India. 30001365

2018

dbSNP: rs1800795
rs1800795
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma
0.010 GeneticVariation BEFREE Subgroup analysis indicated that rs1800795 was significantly associated with increased risk of cervical cancer, colorectal cancer, breast cancer, prostate cancer, lung cancer, glioma, non-Hodgkin's lymphoma and Hodgkin's lymphoma but not gastric cancer and multiple myeloma. 29552316

2018

dbSNP: rs1800795
rs1800795
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.010 GeneticVariation BEFREE The results suggested that the IL-6 rs1800795</span> polymorphism is a protective factor for PCOS susceptibility. 30024552

2018

dbSNP: rs1800795
rs1800795
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.010 GeneticVariation BEFREE Polymorphisms in PITX2 (rs2200733) and IL6 (rs1800795) are associated with postoperative atrial fibrillation in adults but have not been studied in CHD. 29800783

2018

dbSNP: rs1800795
rs1800795
CUI: C1456868
Disease: Diabetic foot ulcer
Diabetic foot ulcer
0.010 GeneticVariation BEFREE The Interleukin (IL)-6 (-174G > C/rs1800795), Tumor Necrosis Factor (TNF)-α (-308G > A/rs1800629) and (-238G > A/rs361525) and Stromal cell Derived Factor (SDF)-1 (+801G > A/rs1801157) are well characterized single nucleotide polymorphisms (SNPs) which were previously shown to be associated with Diabetic Foot Ulcer (DFU). 30009916

2018

dbSNP: rs1800795
rs1800795
CUI: C0003164
Disease: Anthracosilicosis
Anthracosilicosis
0.010 GeneticVariation BEFREE Associations of polymorphisms in the cytokine genes IL1β (rs16944), IL6 (rs1800795), IL12b (rs3212227) and growth factor VEGFA (rs2010963) with anthracosilicosis in coal miners in Russia and related genotoxic effects. 29378067

2018

dbSNP: rs1800795
rs1800795
CUI: C0004936
Disease: Mental disorders
Mental disorders
0.010 GeneticVariation BEFREE In the present study, we genotyped two interleukin 6 (IL-6) variants (rs2069845 and rs1800795) in 320 suicide attempters, 236 suicide completers, and 341 individuals without any history of psychiatric disorders or suicide ideation. 30269203

2018

dbSNP: rs1800795
rs1800795
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver
0.010 GeneticVariation BEFREE Subgroup analyses of rs1800797 also suggested non-significant association and rs1800795 played a protective role in liver cancer. 29842912

2018

dbSNP: rs1800795
rs1800795
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
0.010 GeneticVariation BEFREE In the present study, we genotyped two interleukin 6 (IL-6) variants (rs2069845 and rs1800795) in 320 suicide attempters, 236 suicide completers, and 341 individuals without any history of psychiatric disorders or suicide ideation. 30269203

2018

dbSNP: rs1800795
rs1800795
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 GeneticVariation BEFREE These findings suggest that GG SNP at IL-6: rs1800795 may indicate an increased risk of metastasis of primary breast cancer. 28732081

2017

dbSNP: rs1800795
rs1800795
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE In view of this, the current study aimed to investigate the possible association of 5' promoter polymorphisms G-597A (rs1800797), G-572C (rs1800796) and G-174C (rs1800795) with the risk of SLE. 28530463

2017

dbSNP: rs1800795
rs1800795
Premature coronary artery atherosclerosis
0.010 GeneticVariation BEFREE The risk allele frequencies (RAFs) of rs1800795 <i>(IL6)</i> and rs187238 <i>(IL18)</i> cytokine gene promoter SNPs were significantly higher in the PCAD cases as compared with the controls. 27559091

2017

dbSNP: rs1800795
rs1800795
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.010 GeneticVariation BEFREE In recent years, cytokines and their receptors have been shown to be highly polymorphic, and this prompted us to investigate interleukin 6 promoter polymorphisms at position -174G/C (rs1800795) and at -572G/C (rs1800796) in relation to asthma in children. 28185773

2017

dbSNP: rs1800795
rs1800795
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
0.010 GeneticVariation BEFREE The initial study suggested that GG relative to CG at rs1800795 (OR 1.52; 95% CI 1.14-2.02; p = 0.004) was significantly associated with the development of metastases. 28732081

2017

dbSNP: rs1800795
rs1800795
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 GeneticVariation BEFREE Together, our data support that rs1800795 within the <i>IL</i>-6 gene confers genetic susceptibility for GD. 29228744

2017

dbSNP: rs1800795
rs1800795
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
0.010 GeneticVariation BEFREE IL-6 genotypes of rs1800795 GC and rs1800796 GG might point to a relatively high risk for T2D patients suffering from PDR in a Chinese population and they were associated with elevation of IL-6 expression in both mRNA and protein. 28651253

2017

dbSNP: rs1800795
rs1800795
CUI: C1135196
Disease: Heart Failure, Diastolic
Heart Failure, Diastolic
0.010 GeneticVariation BEFREE The study aimed to assess the clinical significance of selected single nucleotide polymorphisms (SNPs) in patients with diastolic heart failure (HF): inflammation [-174 G/C Interleukin -6 (IL-6) rs1800795, tumor necrosis factor (TNF)-608 G/A rs1800629], fibrosis [Arg25Pro transforming growth factor β (TGF β) rs1800471], endothelial function [-786 T/C nitric oxide synthase (NOS) rs2070744], glucose and lipid metabolism [Pro12Ala peroxisome proliferator activated receptor (PPAR)γ rs1801282], and vitamin D metabolism [cytochrome P450 27B1 (CYP27B1) C-1260A].110 patients with HF with preserved and mid-range ejection fraction (HFpEF and HFmrEF) were recruited. 28827564

2017

dbSNP: rs1800795
rs1800795
CUI: C0035439
Disease: Rheumatic Heart Disease
Rheumatic Heart Disease
0.010 GeneticVariation BEFREE We examined the associations of 8 selected polymorphisms in seven inflammatory genes: IL-6 [rs1800795G/C], IL-10 [rs1800896G/A], TNF-A [rs1800629G/A], IL-1β [rs2853550C/T], IL-1VNTR [rs2234663], TGF-β1 [rs1800469C/T]; [rs1982073T/C], and CTLA-4 [rs5742909C/T] with RHD risk. 27118427

2016

dbSNP: rs1800795
rs1800795
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 GeneticVariation BEFREE To assess the role of Helicobacter pylori infection and interleukin 6 polymorphism -174 (rs1800795) in dyslipidemia. 26781506

2016

dbSNP: rs1800795
rs1800795
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 GeneticVariation BEFREE Our study investigated the frequency of interleukin-6 (IL-6) promoter polymorphism rs1800795 (-174 G>C), possible association of this polymorphism with IL-6 levels and the outcome after stroke in 95 patients with acute ischemic stroke and 268 healthy subjects. 27049557

2016