rs9807989

This variant is located in the IL18R1 gene.

GWAS Catalog Trait Associations (5)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

eosinophil count

Allele C
OR
p 6.0e-305
N 583,850
Large GWAS
multi-ancestry
Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.05
p 4.0e-190
N 442,919
Large GWAS
multi-ancestry
Allele C
OR 0.07
p 8.0e-201
N 394,642
Large GWAS
European

eosinophil percentage of leukocytes

Allele C
OR 0.08
p 9.0e-285
N 394,642
Large GWAS
European
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.05
p 5.0e-48
N 408,112
Large GWAS
European

interleukin-1 receptor type 2 measurement

Allele C
OR 0.06
p 4.0e-26
N 47,745
Large GWAS
European

seasonal allergic rhinitis

Allele C
OR 0.10
p 4.0e-24
N 394,626
Large GWAS
European

eosinophil cationic protein level

Allele C
OR 0.04
p 1.0e-11
N 47,745
Large GWAS
European

About IL18R1

The protein encoded by this gene is a cytokine receptor that belongs to the interleukin 1 receptor family. This receptor specifically binds interleukin 18 (IL18), and is essential for IL18 mediated signal transduction. IFN-alpha and IL12 are reported to induce the expression of this receptor in NK and T cells. This gene along with four other members of the interleukin 1 receptor family, including IL1R2, IL1R1, ILRL2 (IL-1Rrp2), and IL1RL1 (T1/ST2), form a gene cluster on chromosome 2q. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]

View all IL18R1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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