rs1898671

This is a downstream gene variant variant in the TSLP gene.

GWAS Catalog Trait Associations (4)

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

asthma

Ferreira MAR et al. Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. American Journal of Human Genetics 104(4):665-684 (2019)
Allele T
OR 1.10
p 1.0e-38
N 341,215
Large GWAS
European

eosinophil count

Allele T
OR 0.04
p 2.0e-29
N 365,954
Large GWAS
European

Glucocorticoid use measurement

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.10
p 8.0e-20
N 384,426
Large GWAS
multi-ancestry
Allele T
OR 0.10
p 8.0e-17
N 205,700
Major Consortium StudyLarge GWAS
European

asthma, age at onset

Ferreira MAR et al. Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. American Journal of Human Genetics 104(4):665-684 (2019)
Allele T
OR 1.06
p 8.0e-10
N 28,835
Large GWAS
European

About TSLP

This gene encodes a hemopoietic cytokine proposed to signal through a heterodimeric receptor complex composed of the thymic stromal lymphopoietin receptor and the IL-7R alpha chain. It mainly impacts myeloid cells and induces the release of T cell-attracting chemokines from monocytes and enhances the maturation of CD11c(+) dendritic cells. The protein promotes T helper type 2 (TH2) cell responses that are associated with immunity in various inflammatory diseases, including asthma, allergic inflammation and chronic obstructive pulmonary disease. The protein is therefore considered a potential therapeutic target for the treatment of such diseases. In addition, the shorter (predominant) isoform is an antimicrobial protein, displaying antibacterial and antifungal activity against B. cereus, E. coli, E. faecalis, S. mitis, S. epidermidis, and C. albicans. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2020]

View all TSLP variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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