IL9, interleukin 9, 3578

N. diseases: 291; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799962
rs1799962
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0200638
Disease:
Eosinophil count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1859430
rs1859430
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE IL9 polymorphisms (rs11741137, rs2069885, and rs1859430) showed evidence for interaction with dust mite in the Childhood Asthma Management Program (P = .02 to .03), with replication in the Genetics of Asthma in Costa Rica Study (P = .04). 25913104 2015
dbSNP: rs1859430
rs1859430
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0264408
Disease:
Childhood asthma
0.010 GeneticVariation BEFREE IL9 polymorphisms (rs11741137, rs2069885, and rs1859430) showed evidence for interaction with dust mite in the Childhood Asthma Management Program (P = .02 to .03), with replication in the Genetics of Asthma in Costa Rica Study (P = .04). 25913104 2015
dbSNP: rs2069885
rs2069885
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE IL9 polymorphisms (rs11741137, rs2069885, and rs1859430) showed evidence for interaction with dust mite in the Childhood Asthma Management Program (P = .02 to .03), with replication in the Genetics of Asthma in Costa Rica Study (P = .04). 25913104 2015
dbSNP: rs2069885
rs2069885
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0264408
Disease:
Childhood asthma
0.010 GeneticVariation BEFREE IL9 polymorphisms (rs11741137, rs2069885, and rs1859430) showed evidence for interaction with dust mite in the Childhood Asthma Management Program (P = .02 to .03), with replication in the Genetics of Asthma in Costa Rica Study (P = .04). 25913104 2015
dbSNP: rs31564
rs31564
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0014859
Disease:
Esophageal Neoplasms
0.010 GeneticVariation BEFREE We conducted a hospital based case-control study to evaluate the genetic effects of functional single nucleotide polymorphisms (SNPs): interleukin 9 (IL9) rs31563 C>T, IL9 rs31564 G>T, IL10 rs1800872 T>G, IL12A rs2243115 T>G, IL12B rs3212227 T>G and IL13 rs1800925 C>T on the development of esophageal cancer. 23886125 2013
dbSNP: rs31564
rs31564
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0546837
Disease:
Malignant neoplasm of esophagus
0.010 GeneticVariation BEFREE We conducted a hospital based case-control study to evaluate the genetic effects of functional single nucleotide polymorphisms (SNPs): interleukin 9 (IL9) rs31563 C>T, IL9 rs31564 G>T, IL10 rs1800872 T>G, IL12A rs2243115 T>G, IL12B rs3212227 T>G and IL13 rs1800925 C>T on the development of esophageal cancer. 23886125 2013
dbSNP: rs31564
rs31564
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0152018
Disease:
Esophageal carcinoma
0.010 GeneticVariation BEFREE We conducted a hospital based case-control study to evaluate the genetic effects of functional single nucleotide polymorphisms (SNPs): interleukin 9 (IL9) rs31563 C>T, IL9 rs31564 G>T, IL10 rs1800872 T>G, IL12A rs2243115 T>G, IL12B rs3212227 T>G and IL13 rs1800925 C>T on the development of esophageal cancer. 23886125 2013
dbSNP: rs1799962
rs1799962
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0375023
Disease:
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
0.010 GeneticVariation BEFREE Haplotype analysis of two SNPs in the IL-9 gene (rs2069885 and rs1799962) showed overrepresentation of the TT haplotype in girls with severe RSV bronchiolitis requiring hospitalization indicating that this is the haplotype conferring the highest risk in girls. 20503287 2010
dbSNP: rs1799962
rs1799962
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0006271
Disease:
Bronchiolitis
0.010 GeneticVariation BEFREE Haplotype analysis of two SNPs in the IL-9 gene (rs2069885 and rs1799962) showed overrepresentation of the TT haplotype in girls with severe RSV bronchiolitis requiring hospitalization indicating that this is the haplotype conferring the highest risk in girls. 20503287 2010
dbSNP: rs2069885
rs2069885
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0035235
Disease:
Respiratory Syncytial Virus Infections
0.010 GeneticVariation BEFREE Only one SNP (rs2069885) had a gender-specific significant association with RSV infection, severe enough to require hospitalization (P-value 0.00057). 20503287 2010
dbSNP: rs2069885
rs2069885
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0006271
Disease:
Bronchiolitis
0.010 GeneticVariation BEFREE Haplotype analysis of two SNPs in the IL-9 gene (rs2069</span>885 and rs1799962) showed overrepresentation of the TT haplotype in girls with severe RSV bronchiolitis requiring hospitalization indicating that this is the haplotype conferring the highest risk in girls. 20503287 2010
dbSNP: rs2069885
rs2069885
Entrez Id: 3578
Gene Symbol: IL9
IL9
CUI: C0375023
Disease:
Respiratory syncytial virus (RSV) infection in conditions classified elsewhere and of unspecified site
0.010 GeneticVariation BEFREE Haplotype analysis of two SNPs in the IL-9 gene (rs2069</span>885 and rs1799962) showed overrepresentation of the TT haplotype in girls with severe RSV bronchiolitis requiring hospitalization indicating that this is the haplotype conferring the highest risk in girls. 20503287 2010