rs1800925, IL13;TH2LCRR

N. diseases: 37
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neoplasms
CUI: C0027651
Disease: Neoplasms
0.020 GeneticVariation BEFREE Tumor DNA was extracted from these biopsies and sequenced to analyze the rs1800925 polymorphism. 27167201 2016
Rhinitis
CUI: C0035455
Disease: Rhinitis
0.020 GeneticVariation BEFREE A model with rs1058240, rs379568, and rs4143094 (GATA3) and rs1800925 (IL13) and their interactions was selected to predict rhinitis and positive SPT responses. rs1058240 was associated with rhinitis and allergic rhinitis (P < .05), and the gene-gene interaction rs1058240:rs1800925 was associated with rhinitis (P = .043). 18037162 2008
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
0.050 GeneticVariation BEFREE A model with rs1058240, rs379568, and rs4143094 (GATA3) and rs1800925 (IL13) and their interactions was selected to predict rhinitis and positive SPT responses. rs1058240 was associated with rhinitis and allergic rhinitis (P < .05), and the gene-gene interaction rs1058240:rs1800925 was associated with rhinitis (P = .043). 18037162 2008
Psoriasis
CUI: C0033860
Disease: Psoriasis
0.010 GeneticVariation BEFREE A multitiered genetic association study of 25 215 single-nucleotide polymorphisms (SNPs) in three case-control sample sets (1446 patients and 1432 controls) identified three IL13-linked SNPs (rs1800925, rs20541 and rs848) associated with psoriasis. 18075513 2008
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
0.010 GeneticVariation BEFREE Although no SNP was associated with breast cancer risk among women of European descent, we found evidence for an association among East Asians for rs1800925 (IL-13) and breast cancer risk (OR = 2.08; 95% CI: 1.32-3.28; p = 0.000779), which remained statistically significant after multiple testing correction (padj = 0.0350). 30601841 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Although no SNP was associated with breast cancer risk among women of European descent, we found evidence for an association among East Asians for rs1800925 (IL-13) and breast cancer risk (OR = 2.08; 95% CI: 1.32-3.28; p = 0.000779), which remained statistically significant after multiple testing correction (padj = 0.0350). 30601841 2019
Asthma
CUI: C0004096
Disease: Asthma
0.090 GeneticVariation BEFREE Although this SNP (rs1800925) was not associated with asthma exacerbations among all white children in CAMP, it was associated with increased risk of asthma exacerbations among children on inhaled corticosteroids (P = .02). 17561245 2007
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
0.030 GeneticVariation BEFREE An additional SNP, rs1800925, was genotyped only in the PsA and PsC groups. 21613309 2011
Arthritis
CUI: C0003864
Disease: Arthritis
0.010 GeneticVariation BEFREE An additional SNP, rs1800925, was genotyped only in the PsA and PsC groups. 21613309 2011
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
0.020 GeneticVariation BEFREE Association was found between IL-13 gene SNPs (rs20541 and rs1800925) and an increased risk of COPD. 24286397 2013
Appendicitis
CUI: C0003615
Disease: Appendicitis
0.010 GeneticVariation BEFREE Associations with appendicitis were found for SNPs IL-13 rs1800925 with odds ratio (OR) 6.02 (95% CI 1.52-23.78) for T/T versus C/C + T/T, for IL-17 rs2275913 with OR 2.38 (CI 1.24-4.57) for A/A vs G/G + GA, for CCL22 rs223888 with OR 0.12 (0.02-0.90), and for A/A vs G/G + GA. Signs of effect modification of age for the association with appendicitis were found for IL-13 rs1800925 and CTLA4 rs3087243. 31845023 2020
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
0.030 GeneticVariation BEFREE Both SNPs were found to be highly associated with susceptibility to PsA (rs1800925 ptrend = 6.1 × 10(-5) OR 1.33, rs20541 ptrend = 8.0 × 10(-4) OR 1.27), but neither SNP was significantly associated with susceptibility to PsV. 21349879 2011
Psoriasis vulgaris
CUI: C0263361
Disease: Psoriasis vulgaris
0.010 GeneticVariation BEFREE Both SNPs were found to be highly associated with susceptibility to PsA (rs1800925 ptrend = 6.1 × 10(-5) OR 1.33, rs20541 ptrend = 8.0 × 10(-4) OR 1.27), but neither SNP was significantly associated with susceptibility to PsV. 21349879 2011
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
0.010 GeneticVariation BEFREE Can an IL13 -1112 C/T (rs1800925) polymorphism predict responsiveness to neoadjuvant chemoradiotherapy and survival of Chinese Han patients with locally advanced rectal cancer? 27167201 2016
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
0.050 GeneticVariation BEFREE However, a recent meta-analysis using data from these 6 studies has shown that the A allele of IL13 SNP rs20541 was associated with an increased risk of allergic rhinitis, whereas no such relationship existed between IL13 SNP rs1800925 and allergic rhinitis. 22023794 2011
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
0.010 GeneticVariation BEFREE However, stratification analyses suggested that the IL-13 rs1800925 CT and CT/CC genotypes increased the risk of RA in patients with erythrocyte sedimentation rate (ESR) <25.00. 27323078 2016
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
0.050 GeneticVariation BEFREE However, the accumulating evidence does not support an association of IL-13 SNP rs1800925 and CD14 SNP rs2569190 with AR risk. 29687183 2018
Rhinitis
CUI: C0035455
Disease: Rhinitis
0.020 GeneticVariation BEFREE IL13 C-1111T (rs1800925) was significantly associated with rhinitis and atopic phenotypes in rhinitis trios that were not affected by clinical asthma. 20484924 2010
Asthma
CUI: C0004096
Disease: Asthma
0.090 GeneticVariation BEFREE IL13 C-1111T (rs1800925) was significantly associated with rhinitis and atopic phenotypes in rhinitis trios that were not affected by clinical asthma. 20484924 2010
Asthma
CUI: C0004096
Disease: Asthma
0.090 GeneticVariation BEFREE IL13 encodes IL-13, a Th2 cytokine, and rs1800925 and rs20541 confer risk of asthma. 19554022 2009
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
0.050 GeneticVariation BEFREE IL13 SNP rs1800925 and IL4R SNP 1801275 did not demonstrate overall associations with AR. 21309855 2011
Asthma
CUI: C0004096
Disease: Asthma
0.090 GeneticVariation BEFREE IL13 SNPs rs1881457(-1512) and rs1800925(-1111) were associated with better FEV(1) and FEV(1)/FVC in asthmatics. 19796199 2010
Rhinoconjunctivitis
CUI: C0861155
Disease: Rhinoconjunctivitis
0.010 GeneticVariation BEFREE In addition, a new pattern of biological interaction that affects the risk of rhinoconjunctivitis is described between SNP rs1800925 and smoking. 22023794 2011
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
0.010 GeneticVariation BEFREE In conclusion, the rs1800925 T allele of the IL-13 gene is associated with worse pulmonary function in patients with IPF of Chinese Han ethnicity. 23549736 2013
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
0.020 GeneticVariation BEFREE In subgroup analysis according to ethnicity, the T allele of rs1800925 was associated with an increased risk of COPD in Asians (OR = 1.88, 95% CI: 1.23-2.87, Pz = .004) and Caucasians (OR = 1.30, 95% CI: 1.01-1.67, Pz = .041), respectively. 29381928 2017