IL1RN, interleukin 1 receptor antagonist, 3557

N. diseases: 701; N. variants: 52
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs454078
rs454078
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C3815172
Disease:
Interleukin 1 Beta Measurement
0.700 GeneticVariation GWASCAT GWAS for Interleukin-1β levels in gingival crevicular fluid identifies IL37 variants in periodontal inflammation. 30206230 2018
dbSNP: rs495282
rs495282
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C3815172
Disease:
Interleukin 1 Beta Measurement
0.700 GeneticVariation GWASCAT GWAS for Interleukin-1β levels in gingival crevicular fluid identifies IL37 variants in periodontal inflammation. 30206230 2018
dbSNP: rs495410
rs495410
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C3815172
Disease:
Interleukin 1 Beta Measurement
0.700 GeneticVariation GWASCAT GWAS for Interleukin-1β levels in gingival crevicular fluid identifies IL37 variants in periodontal inflammation. 30206230 2018
dbSNP: rs55709272
rs55709272
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C1445957
Disease:
Serum total cholesterol measurement
T 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs10171849
rs10171849
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0200633
Disease:
Neutrophil count (procedure)
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2029582
rs2029582
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0200633
Disease:
Neutrophil count (procedure)
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2029582
rs2029582
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0200641
Disease:
Blood basophil count (lab test)
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2029582
rs2029582
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0200638
Disease:
Eosinophil count procedure
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2029582
rs2029582
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0857490
Disease:
Granulocyte count
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4252040
rs4252040
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0428472
Disease:
Serum HDL cholesterol measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs4252040
rs4252040
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0392885
Disease:
High density lipoprotein measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs121913161
rs121913161
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C2748507
Disease:
INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY
T 0.700 CausalMutation CLINVAR
dbSNP: rs121913162
rs121913162
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C2748507
Disease:
INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY
T 0.700 CausalMutation CLINVAR
dbSNP: rs315952
rs315952
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0035222
Disease:
Respiratory Distress Syndrome, Adult
0.020 GeneticVariation BEFREE We hypothesized that a synonymous coding variant in the IL-1 receptor antagonist gene (IL1RN), rs315952, previously associated with reduced risk for acute respiratory distress syndrome, would be functional and associate with improved survival in septic shock. 25089931 2014
dbSNP: rs315952
rs315952
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.020 GeneticVariation BEFREE Polymorphism in IL-1RN rs315952 was significantly associated with SLE in Iranian patients, rs315952CT genotype being a protective factor. 23722873 2013
dbSNP: rs315952
rs315952
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0035222
Disease:
Respiratory Distress Syndrome, Adult
0.020 GeneticVariation BEFREE A total of 12 SNPs met the stage I threshold for an association with ARDS. rs315952 in the IL1RN gene encoding IL-1 receptor antagonist (IL1RA) replicated its association with reduced ARDS risk in stages II (P < 0.004) and III (P < 0.02), and was robust to clinical adjustment (combined odds ratio = 0.81; P = 4.2 × 10(-5)). 23449693 2013
dbSNP: rs315952
rs315952
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.020 GeneticVariation BEFREE Our results showed that IL1RN (rs315952) was significantly associated with SLE in patients without renal disorder in the family-based study, after disease stratification, but was not significantly associated with SLE in the case-control study. 17176440 2006
dbSNP: rs2234663
rs2234663
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0151779
Disease:
Cutaneous Melanoma
0.010 GeneticVariation BEFREE The present study investigated whether a variable number tandem repeat (VNTR) polymorphism of interleukin-1 receptor antagonist (IL-1RA) gene (<i>IL-1RN</i>) located in intron 2 (rs2234663) is associated with cutaneous melanoma. 31788049 2019
dbSNP: rs2234663
rs2234663
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0023283
Disease:
Leishmaniasis, Cutaneous
0.010 GeneticVariation BEFREE The SNPs -511T/C (rs16944) and +3954C/T (rs1143634) of the IL1B and IL1RN VNTR (rs2234663) were assessed in 881 patients with CL and 837 healthy controls by PCR-RFLP and direct PCR respectively. 31357078 2019
dbSNP: rs2234663
rs2234663
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0041228
Disease:
African Trypanosomiasis
0.010 GeneticVariation BEFREE This study revealed that one SNP rs1800794 of IL1A and one VNTR rs2234663 of IL1RN were associated with the increased risk to be infected by Trypanosoma brucei gambiense and develop sleeping sickness in southern Cameroon. 30908482 2019
dbSNP: rs2234663
rs2234663
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0025202
Disease:
melanoma
0.010 GeneticVariation BEFREE The present study investigated whether a variable number tandem repeat (VNTR) polymorphism of interleukin-1 receptor antagonist (IL-1RA) gene (<i>IL-1RN</i>) located in intron 2 (rs2234663) is associated with cutaneous melanoma. 31788049 2019
dbSNP: rs315919
rs315919
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0546837
Disease:
Malignant neoplasm of esophagus
0.010 GeneticVariation BEFREE Our study provided the first evidence that IL1RN rs3181052, rs452204, and rs315919 are correlated with a decreased risk of esophageal cancer in a Northwest Han Chinese population. 30995661 2019
dbSNP: rs315919
rs315919
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0014859
Disease:
Esophageal Neoplasms
0.010 GeneticVariation BEFREE Our study provided the first evidence that IL1RN rs3181052, rs452204, and rs315919 are correlated with a decreased risk of esophageal cancer in a Northwest Han Chinese population. 30995661 2019
dbSNP: rs315919
rs315919
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0152018
Disease:
Esophageal carcinoma
0.010 GeneticVariation BEFREE Our study provided the first evidence that IL1RN rs3181052, rs452204, and rs315919 are correlated with a decreased risk of esophageal cancer in a Northwest Han Chinese population. 30995661 2019
dbSNP: rs3181052
rs3181052
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
CUI: C0014859
Disease:
Esophageal Neoplasms
0.010 GeneticVariation BEFREE In stratified analyses </span>by age >55 years, rs3181052 reduced the risk of esophageal cancer in the dominant and overdominant models. 30995661 2019