rs7555082

This is a intergenic variant variant.

GWAS Catalog Trait Associations (6)

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

lymphocyte percentage of leukocytes

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.03
p 3.0e-14
N 408,112
Large GWAS
European

Crohn's disease

Allele A
OR 1.13
p 1.0e-10
N 20,883
Large GWAS
multi-ancestry

Inhalant adrenergic 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 A
OR 0.08
p 5.0e-9
N 355,171
Large GWAS
multi-ancestry

hyperthyroidism

Figuerêdo J et al. Uncovering the shared genetic components of thyroid disorders and reproductive health. European Journal of Endocrinology 191(2):211-222 (2024)
Allele G
OR 1.20
p 7.0e-9
N 743,008
Large GWAS
European

This variant is in our database but has no known associations or PRS memberships yet.

Gene information from NCBI Gene. Variant classifications from ClinVar.

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