IL2, interleukin 2, 3558

N. diseases: 950; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2069772
rs2069772
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0018621
Disease:
Hay fever
C 0.800 GeneticVariation GWASDB A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order. 22036096 2011
dbSNP: rs2069772
rs2069772
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0018621
Disease:
Hay fever
C 0.800 GeneticVariation GWASCAT A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order. 22036096 2011
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
0.710 GeneticVariation BEFREE Our aim was to evaluate the association of the four IL2 polymorphisms (rs6822844, rs6534349, rs2069762 and rs3136534) with type 1 diabetes (T1D) in the Polish population, and to correlate them with the serum interleukin-2 levels. 24154763 2013
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
A 0.710 GeneticVariation GWASCAT Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. 21829393 2011
dbSNP: rs2069763
rs2069763
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0264408
Disease:
Childhood asthma
A 0.700 GeneticVariation GWASCAT Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. 31036433 2019
dbSNP: rs2069772
rs2069772
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0007570
Disease:
Celiac Disease
0.700 GeneticVariation GWASCAT Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci. 25920553 2016
dbSNP: rs2069772
rs2069772
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C1527304
Disease:
Allergic Reaction
C 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C1272321
Disease:
Autoantibody measurement
A 0.700 GeneticVariation GWASDB Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. 21829393 2011
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0041296
Disease:
Tuberculosis
0.010 GeneticVariation BEFREE Collectively, this meta-analysis proved that IL-2 rs2069762, IL-4 rs2243250, IL-6 rs1800795, IL-8 rs4073, IL-10 rs1800871 and IL-10 rs1800896 polymorphisms may confer susceptibility to TB, especially for Asians. 31669382 2020
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE Kaplan-Meier analysis showed that cancer-specific survival was worse for individuals with C allele for rs2069762 with stage II CRC and with T allele for rs6822844 with stage III CRC. 31519598 2019
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0015230
Disease:
Exanthema
0.010 GeneticVariation BEFREE However, we demonstrated an association between the SNP in IL2 (rs2069762) and the onset of skin rash (P = 0·0001). 30203425 2019
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0023449
Disease:
Acute lymphocytic leukemia
0.010 GeneticVariation BEFREE The purpose of this work was to explore the association of IFNG +874 A/T (rs2430561) and IL2 -330 G/T (rs2069762) SNPs with ALL susceptibility and/or protection in 488 Mexican Mestizos patients, as compared to 950 Mexican Mestizo healthy controls. 30212785 2018
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C4721555
Disease:
Autoimmune hepatitis
0.010 GeneticVariation BEFREE G/T alleles of IL-2 at -330 (rs2069762) and A/T alleles on UTR +5644 position at IFN-γ and their subsequent haplotypes, did not show significant association with AIH. 29288086 2018
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0019069
Disease:
Hemophilia A
0.010 GeneticVariation BEFREE Polymorphisms in the TGF-β1 (rs1982037) and IL-2 (rs2069762, rs4833248) genes are not associated with inhibitor development in Iranian patients with hemophilia A. 29993342 2018
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0023452
Disease:
Childhood Acute Lymphoblastic Leukemia
0.010 GeneticVariation BEFREE The purpose of this work was to explore the association of IFNG +874 A/T (rs2430561) and IL2 -330 G/T (rs2069762) SNPs with ALL susceptibility and/or protection in 488 Mexican Mestizos patients, as compared to 950 Mexican Mestizo healthy controls. 30212785 2018
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0751606
Disease:
Adult Acute Lymphocytic Leukemia
0.010 GeneticVariation BEFREE The purpose of this work was to explore the association of IFNG +874 A/T (rs2430561) and IL2 -330 G/T (rs2069762) SNPs with ALL susceptibility and/or protection in 488 Mexican Mestizos patients, as compared to 950 Mexican Mestizo healthy controls. 30212785 2018
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0241910
Disease:
Autoimmune Chronic Hepatitis
0.010 GeneticVariation BEFREE G/T alleles of IL-2 at -330 (rs2069762) and A/T alleles on UTR +5644 position at IFN-γ and their subsequent haplotypes, did not show significant association with AIH. 29288086 2018
dbSNP: rs2069763
rs2069763
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0241910
Disease:
Autoimmune Chronic Hepatitis
0.010 GeneticVariation BEFREE IL-2 T allele at position +166 (rs2069763) showed significant higher frequency in AIH group (36%), compared to the controls (21%) (OR=2.06; 95% CI, 1.24-3.43, P-value<0.01). 29288086 2018
dbSNP: rs2069763
rs2069763
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C4721555
Disease:
Autoimmune hepatitis
0.010 GeneticVariation BEFREE IL-2 T allele at position +166 (rs2069763) showed significant higher frequency in AIH group (36%), compared to the controls (21%) (OR=2.06; 95% CI, 1.24-3.43, P-value<0.01). 29288086 2018
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0271907
Disease:
Acquired aplastic anemia
0.010 GeneticVariation BEFREE It could be assumed that the rs2069762 polymorphism might reduce the risk of acquired aplastic anemia, while the remaining four SNPs might not contribute to susceptibility to acquired AA in a Chinese population. 28268223 2017
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.010 GeneticVariation BEFREE Based on the genetic characteristics of the studied individuals, the interaction between IL2 rs2069762 and nonfermented soy intake may modify the risk of gastric cancer. 28111424 2017
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0699791
Disease:
Stomach Carcinoma
0.010 GeneticVariation BEFREE Based on the genetic characteristics of the studied individuals, the interaction between IL2 rs2069762 and nonfermented soy intake may modify the risk of gastric cancer. 28111424 2017
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0041327
Disease:
Tuberculosis, Pulmonary
0.010 GeneticVariation BEFREE The aim of this study was to evaluate the association between previously reported SNPs IL2-330 T>G (rs2069762); IL4-590 C>T (rs2243250); IL6-174 G>C (rs1800795); IL10-592 A>C (rs1800872); IL10-1082 G>A (rs1800896); IL17A -692 C>T (rs8193036); IL17A -197 G>A (rs2275913); TNF -238 G>A (rs361525); TNF -308 G>A (rs1800629) and IFNG +874 T>A (rs2430561) and pulmonary TB (PTB) susceptibility. 26840977 2016
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C0033860
Disease:
Psoriasis
0.010 GeneticVariation BEFREE Our data indicated that rs2069762 GG, TG genotypes [GG: odds ratio (OR) = 2.6875, 95% confidence interval (CI) = 1.5948-4.5290, P < 0.0001; TG: OR = 1.6159, 95% CI = 1.2044-2.1681, P = 0.0013], and H3 haplotype (OR = 1.717, 95% CI = 1.050-2.808, P = 0.030) increased the risk of psoriasis. 25495849 2015
dbSNP: rs2069762
rs2069762
Entrez Id: 3558
Gene Symbol: IL2
IL2
CUI: C1302547
Disease:
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
0.010 GeneticVariation BEFREE For diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL), and chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), joint associations of body mass index (from self-reported height and weight) and 12 polymorphisms in cytokines IL1A (rs1800587), IL1B (rs16944, rs1143627), IL1RN (rs454078), IL2 (rs2069762), IL6 (rs1800795, rs1800797), IL10 (rs1800890, rs1800896), TNF (rs1800629), LTA (rs909253), and CARD15 (rs2066847) were investigated using unconditional logistic regression. 25962811 2015