IL10, interleukin 10, 3586

N. diseases: 1679; N. variants: 21
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800872
rs1800872
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
G 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs3021094
rs3021094
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0085207
Disease:
Gestational Diabetes
0.010 GeneticVariation BEFREE <b>Conclusion:</b> Our study demonstrated that A allele and A/A genotype of rs3021094 SNP in IL-10 gene were linked to increased risk for GDM, IL-10 plasma level and insulin resistance, which could be potential targets for early screening and detection of GDM. 30873205 2019
dbSNP: rs1800872
rs1800872
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0085207
Disease:
Gestational Diabetes
0.020 GeneticVariation BEFREE <b>Results:</b> There were no statistically significant differences in the distribution of <i>IL-1β</i> rs16944 and <i>IL-10</i> rs1800872 between GDM and healthy women. 31630588 2019
dbSNP: rs1800896
rs1800896
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0041327
Disease:
Tuberculosis, Pulmonary
0.020 GeneticVariation BEFREE <i>IL-10</i> -1082 A>G (rs1800896) polymorphism confers susceptibility to pulmonary tuberculosis in Caucasians but not in Asians and Africans: a meta-analysis. 28951522 2017
dbSNP: rs1800871
rs1800871
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C3160901
Disease:
Behcet's uveitis
0.010 GeneticVariation BEFREE <i>Results</i>: The risk allele, A, in rs1800871, of <i>IL-10</i> gene was highly prevalent in Behcet's uveitis and healthy control samples alike; highest among the Turkish groups. 29792538 2019
dbSNP: rs1800896
rs1800896
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C1848934
Disease:
SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME
0.010 GeneticVariation BEFREE SCT and IL10 rs1800896, IL1A rs2856838, but not SEMA3C rs4461841, polymorphisms were associated with decreased risk of malaria in the controls. 29033373 2017
dbSNP: rs145922845
rs145922845
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0010346
Disease:
Crohn Disease
0.030 GeneticVariation BEFREE A Gly15Arg mutation in the leader sequence of IL-10 was found in a multiple CD-affected family. 12825869 2003
dbSNP: rs1800896
rs1800896
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0009402
Disease:
Colorectal Carcinoma
0.040 GeneticVariation BEFREE A case-control study of 401 cases and 300 sex- and age-matched controls was performed in order to explore the role of IL1B_1473G/C (rs1143623), SOD1_7958A/G (rs4998557), TLR4_1196C/T (rs4986791), IL10_1082A/G (rs1800896), IL17A_197G/A (rs2275913), and TLR4_896A/G (rs4986790) polymorphisms in the susceptibility to colorectal cancer (n = 244), gastric carcinoma (n = 72), and ovarian cancer (n = 85). 24446182 2014
dbSNP: rs1800896
rs1800896
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum
0.020 GeneticVariation BEFREE A case-control study of 401 cases and 300 sex- and age-matched controls was performed in order to explore the role of IL1B_1473G/C (rs1143623), SOD1_7958A/G (rs4998557), TLR4_1196C/T (rs4986791), IL10_1082A/G (rs1800896), IL17A_197G/A (rs2275913), and TLR4_896A/G (rs4986790) polymorphisms in the susceptibility to colorectal cancer (n = 244), gastric carcinoma (n = 72), and ovarian cancer (n = 85). 24446182 2014
dbSNP: rs1800872
rs1800872
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0009402
Disease:
Colorectal Carcinoma
0.040 GeneticVariation BEFREE A decreased risk of colorectal cancer in subjects with rs1800872 AC genotype of IL10 (OR = 0.643, 95%CI = 0.453, 0.912) or AC/CC genotype (OR = 0.636, 95%CI = 0.457, 0.885) was observed, compared with those with AA genotype. 24762198 2014
dbSNP: rs1800872
rs1800872
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C4722085
Disease:
Malignant neoplasm of colon and/or rectum
0.010 GeneticVariation BEFREE A decreased risk of colorectal cancer in subjects with rs1800872 AC genotype of IL10 (OR = 0.643, 95%CI = 0.453, 0.912) or AC/CC genotype (OR = 0.636, 95%CI = 0.457, 0.885) was observed, compared with those with AA genotype. 24762198 2014
dbSNP: rs3024493
rs3024493
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
0.700 GeneticVariation GWASDB A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci. 21980299 2011
dbSNP: rs1800896
rs1800896
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.020 GeneticVariation BEFREE A large number of studies have shown that the -1082A/G polymorphism (rs1800896) in the Interleukin-10 gene (IL-10) is implicated in the susceptibility to rheumatoid arthritis (RA). 21764596 2011
dbSNP: rs1800872
rs1800872
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0686619
Disease:
Secondary malignant neoplasm of lymph node
0.010 GeneticVariation BEFREE A promoter variant (rs1800872) in the Interleukin-10 (IL-10) gene was associated with an increased lymph node metastasis involvement [odds ratio (OR) = 2.1, 95% confidence interval (CI) = 1.03-4.2, for carriers of the TT genotype]. 21239167 2011
dbSNP: rs1800896
rs1800896
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0021390
Disease:
Inflammatory Bowel Diseases
0.030 GeneticVariation BEFREE A total of 101 patients diagnosed with inflammatory bowel disease were analysed for the tumour necrosis factor-alpha (-308 G/A; rs1800629) and interleukin-10 (-1082 G/A; rs1800896) gene polymorphisms. 27528546 2016
dbSNP: rs1800896
rs1800896
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C2931822
Disease:
Nasopharyngeal carcinoma
0.030 GeneticVariation BEFREE A total of 698 native Taiwanese consisting of 176 cases and 522 controls were enrolled in this hospital-based study, and three single-nucleotide polymorphism sites at promoter regions of IL10, A-1082G (rs1800896), T-819C (rs3021097), and A-592C (rs1800872) were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and their interaction with smoking habit for NPC risk were evaluated. 23898109 2013
dbSNP: rs3021097
rs3021097
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C2931822
Disease:
Nasopharyngeal carcinoma
0.010 GeneticVariation BEFREE A total of 698 native Taiwanese consisting of 176 cases and 522 controls were enrolled in this hospital-based study, and three single-nucleotide polymorphism sites at promoter regions of IL10, A-1082G (rs1800896), T-819C (rs3021097), and A-592C (rs1800872) were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and their interaction with smoking habit for NPC risk were evaluated. 23898109 2013
dbSNP: rs1800872
rs1800872
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C2931822
Disease:
Nasopharyngeal carcinoma
0.020 GeneticVariation BEFREE A total of 698 native Taiwanese consisting of 176 cases and 522 controls were enrolled in this hospital-based study, and three single-nucleotide polymorphism sites at promoter regions of IL10, A-1082G (rs1800896), T-819C (rs3021097), and A-592C (rs1800872) were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and their interaction with smoking habit for NPC risk were evaluated. 23898109 2013
dbSNP: rs1800896
rs1800896
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C1332986
Disease:
Childhood Osteosarcoma
0.010 GeneticVariation BEFREE Additionally, a statistically significant association between the IL-10 -1082A/G (rs1800896) genotype and poor survival in osteosarcoma</span> patients was observed. 26503210 2016
dbSNP: rs1800896
rs1800896
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0029463
Disease:
Osteosarcoma
0.010 GeneticVariation BEFREE Additionally, a statistically significant association between the IL-10 -1082A/G (rs1800896) genotype and poor survival in osteosarcoma</span> patients was observed. 26503210 2016
dbSNP: rs1800896
rs1800896
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0585442
Disease:
Osteosarcoma of bone
0.010 GeneticVariation BEFREE Additionally, a statistically significant association between the IL-10 -1082A/G (rs1800896) genotype and poor survival in osteosarcoma</span> patients was observed. 26503210 2016
dbSNP: rs1800871
rs1800871
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C1997217
Disease:
Low grade glioma
0.010 GeneticVariation BEFREE Additionally, univariate (Log-rank p = 0.019) and multivariate Cox regression analyses (p = 0.022) showed that the IL-10 rs1800871 C/T genotype correlates with improved overall survival in cases of low-grade glioma, whereas the PRKDC rs7003908 C/C genotype correlated with reduced overall and progression-free survival in high-grade glioma patients in univariate (Log-rank p = 0.000 and p = 0.000, respectively) and multivariate Cox regression analyses (p = 0.001; p = 0.002, respectively). 27811370 2016
dbSNP: rs1800871
rs1800871
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C2349952
Disease:
Oropharyngeal Carcinoma
0.010 GeneticVariation BEFREE After adjusting for age, education, ethnicity, gender, and tobacco smoking, IL10 rs1800871 was inversely associated with oropharyngeal cancer (CT+TT vs. CC adjusted odds ratio [aOR]: 0.69, 95% confidence interval [CI]: 0.50-0.95), and was positively associated with lung cancer among never smokers (TT vs. CT+CC aOR: 2.5, 95% CI: 1.3-5.1) and inversely with oropharyngeal cancer among ever smokers (CT+TT vs. CC aOR: 0.63, 95% CI: 0.41-0.95). 20112337 2010
dbSNP: rs1800871
rs1800871
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0153382
Disease:
Malignant neoplasm of oropharynx
0.010 GeneticVariation BEFREE After adjusting for age, education, ethnicity, gender, and tobacco smoking, IL10 rs1800871 was inversely associated with oropharyngeal cancer (CT+TT vs. CC adjusted odds ratio [aOR]: 0.69, 95% confidence interval [CI]: 0.50-0.95), and was positively associated with lung cancer among never smokers (TT vs. CT+CC aOR: 2.5, 95% CI: 1.3-5.1) and inversely with oropharyngeal cancer among ever smokers (CT+TT vs. CC aOR: 0.63, 95% CI: 0.41-0.95). 20112337 2010
dbSNP: rs1800871
rs1800871
Entrez Id: 3586;29949
Gene Symbol: IL10;IL19
IL10;IL19
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE After adjusting for age, education, ethnicity, gender, and tobacco smoking, IL10 rs1800871 was inversely associated with oropharyngeal cancer (CT+TT vs. CC adjusted odds ratio [aOR]: 0.69, 95% confidence interval [CI]: 0.50-0.95), and was positively associated with lung cancer among never smokers (TT vs. CT+CC aOR: 2.5, 95% CI: 1.3-5.1) and inversely with oropharyngeal cancer among ever smokers (CT+TT vs. CC aOR: 0.63, 95% CI: 0.41-0.95). 20112337 2010