IL13, interleukin 13, 3596

N. diseases: 587; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800925
rs1800925
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
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
dbSNP: rs1800925
rs1800925
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
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
dbSNP: rs1800925
rs1800925
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
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
dbSNP: rs20541
rs20541
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0686619
Disease:
Secondary malignant neoplasm of lymph node
0.010 GeneticVariation BEFREE Our results, the first report, provide evidence that rs20541 polymorphisms may affect the lymph node metastasis of NPC patients in Chinese population. 30472105 2019
dbSNP: rs20541
rs20541
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0018572
Disease:
Hand, Foot and Mouth Disease
0.010 GeneticVariation BEFREE The G allele at the rs20541 locus of IL-13 gene and the A allele at the rs179019 locus of the TLR-7 gene were not risk factors for severe HFMD in either male or female patients. 30807256 2019
dbSNP: rs1800925
rs1800925
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE Our results indicate IL-13 SNP rs1800925 as a risk factor for CRC and that IL-4 SNP rs2243250 could be a useful prognostic marker in the follow-up and clinical management of patients with CRC especially in stage III disease. 30227113 2018
dbSNP: rs20541
rs20541
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE Here, we studied the genetic role of IL-13 in CAD in a Chinese Han population using tag SNPs covering the whole IL13 gene (i.e., rs1881457, rs2069744 and rs20541) and a two-stage cohort containing 1863 CAD cases and 1841 controls. 29670225 2018
dbSNP: rs20541
rs20541
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0035455
Disease:
Rhinitis
0.010 GeneticVariation BEFREE To evaluate whether polymorphisms of IL4R (rs1805015), IL13 (rs20541), IL17A (rs2275913) and GSTP1 (rs1695) genes are associated with rhinitis and/or asthma in adults of Portuguese ancestry. 27561723 2018
dbSNP: rs20541
rs20541
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE These results suggest that rs2</span>0541 CT/TT genotypes may be a risk factor for SLE, probably by increasing the level of IL-13. 29017771 2018
dbSNP: rs1295686
rs1295686
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C4554344
Disease:
IgE-mediated food allergy
0.010 GeneticVariation BEFREE We show for the first time, in two independent cohorts, that IL13 polymorphism rs1295686 (in complete linkage disequilibrium with functional variant rs20541) is associated with challenge-proven food allergy. 28544327 2017
dbSNP: rs20541
rs20541
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C4554344
Disease:
IgE-mediated food allergy
0.010 GeneticVariation BEFREE We show for the first time, in two independent cohorts, that IL13 polymorphism rs1295686 (in complete linkage disequilibrium with functional variant rs20541) is associated with challenge-proven food allergy. 28544327 2017
dbSNP: rs20541
rs20541
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0009766
Disease:
Allergic Conjunctivitis
0.010 GeneticVariation BEFREE Our aim was to observe factors associated with IL13 rs20541 polymorphism and other factors with or without allergic comorbidities such as subject-reported allergic rhinitis (AR) and/or allergic conjunctivitis (AC) symptoms in adult asthmatics. 28273659 2017
dbSNP: rs20541
rs20541
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0267026
Disease:
Actinic cheilitis
0.010 GeneticVariation BEFREE Our aim was to observe factors associated with IL13 rs20541 polymorphism and other factors with or without allergic comorbidities such as subject-reported allergic rhinitis (AR) and/or allergic conjunctivitis (AC) symptoms in adult asthmatics. 28273659 2017
dbSNP: rs848
rs848
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE Although the three SNPs showed no statistically significant associations with the risk and prognosis of CRC, a significant antagonistic interaction was found between rs848 (G-T) and allium vegetable intake (ORi (odds ratio of interaction), 0.92; 95% CI (confidence interval): 0.86, 0.99; P = 0.03); moreover, significant combined and synergistic interactions were observed for all three SNPs and overnight meal intake. 28537887 2017
dbSNP: rs1800925
rs1800925
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
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
dbSNP: rs1800925
rs1800925
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
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
dbSNP: rs1800925
rs1800925
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0266929
Disease:
Chronic Periodontitis
0.010 GeneticVariation BEFREE No significant association between rs2070874 or rs1800925 and CP was found, while the frequencies of rs2243248 and two haplotypes C-G-T and C-T-T showed significant differences between the two groups. 27195298 2016
dbSNP: rs20541
rs20541
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0694549
Disease:
Community acquired pneumonia
0.010 GeneticVariation BEFREE We studied common polymorphisms in the genes of proinflammatory cytokines (IL6 rs1800795, IL8 rs4073, IL1B rs16944), anti-inflammatory cytokines (IL10 rs1800896, IL4 rs2243250, IL13 rs20541) and toll-like receptors (TLR2 rs5743708 and rs4696480, TLR4 rs4986791, TLR9 rs352139, rs5743836 and rs187084) in patients with community-acquired pneumonia (CAP) (390 cases, 203 controls) and nosocomial pneumonia (355 cases, 216 controls). 27725770 2016
dbSNP: rs20541
rs20541
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0264408
Disease:
Childhood asthma
0.010 GeneticVariation BEFREE Each of the four SNPs was identified to have an independent association with childhood asthma (G allele of rs20541, odds ratio (OR) = 1.24, P = 1.23E-03; T allele of rs2243250, OR = 1.25, P = 3.81E-03; A allele of rs1042713, OR = 1.29, P = 6.75E-05; G allele of rs569108, OR = 1.27, P = 3.86E-03). 26613553 2016
dbSNP: rs20541
rs20541
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C1855179
Disease:
CATARACT, ANTERIOR POLAR
0.010 GeneticVariation BEFREE We studied common polymorphisms in the genes of proinflammatory cytokines (IL6 rs1800795, IL8 rs4073, IL1B rs16944), anti-inflammatory cytokines (IL10 rs1800896, IL4 rs2243250, IL13 rs20541) and toll-like receptors (TLR2 rs5743708 and rs4696480, TLR4 rs4986791, TLR9 rs352139, rs5743836 and rs187084) in patients with community-acquired pneumonia (CAP) (390 cases, 203 controls) and nosocomial pneumonia (355 cases, 216 controls). 27725770 2016
dbSNP: rs848
rs848
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE After adjusting for multiple testing and potential confounders, SNP rs848 in the IL13 gene region is significantly associated with a continuous measure of symptom severity in adult subjects with ever asthma. 26986948 2016
dbSNP: rs1295686
rs1295686
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C4531177
Disease:
Sleep onset Insomnia
0.010 GeneticVariation BEFREE After adjusting for genomic estimates of ancestry, self-reported race/ethnicity and viral load, SOI was associated with higher IL-13 plasma levels and with six single nucleotide polymorphisms (SNPs): IL1B rs1143642 and rs1143623, IL6 rs4719714, IL13 rs1295686, NFKB1 rs4648110, and TNFA rs2857602. 25535857 2015
dbSNP: rs1800925
rs1800925
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0023530
Disease:
Leukopenia
0.010 GeneticVariation BEFREE The T allele in IL13 rs1800925 was associated with an increase in the risk of leukopenia (OR = 6.76, 95 % CI = 1.35-33.9, P = 0.020) and increased prevalence of any toxicity > grade 2 (OR = 1.75, 95 % CI = 1.06-2.88, P = 0.028). 26387812 2015
dbSNP: rs1800925
rs1800925
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C0019163
Disease:
Hepatitis B
0.010 GeneticVariation BEFREE This study was undertaken to determine the relationship between two IL-13 gene single nucleotide polymorphisms (SNP rs1800925 and SNP rs20541) and the incidence of hepatitis B virus-related (HBV) hepatocellular carcinoma (HCC). 25658755 2015
dbSNP: rs1800925
rs1800925
Entrez Id: 3596;101927761
Gene Symbol: IL13;TH2LCRR
IL13;TH2LCRR
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE This study was undertaken to determine the relationship between two IL-13 gene single nucleotide polymorphisms (SNP rs1800925 and SNP rs20541) and the incidence of hepatitis B virus-related (HBV) hepatocellular carcinoma (HCC). 25658755 2015