rs11769630

This is a intergenic variant variant.

GWAS Catalog Trait Associations (10)

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

granulocyte percentage of myeloid white cells

Allele A
OR 0.11
p 2.0e-54
N 169,545
Large GWAS
European

neutrophil 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 0.05
p 5.0e-35
N 408,112
Large GWAS
European
Allele A
OR 0.05
p 1.0e-14
N 171,542
Large GWAS
European

C-type lectin domain family 5 member A measurement

Allele A
OR 0.10
p 5.0e-25
N 47,745
Large GWAS
European

platelet component distribution width

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele A
OR 0.04
p 1.0e-16
N 408,112
Large GWAS
European

fms-related tyrosine kinase 3 ligand measurement

Allele A
OR 0.07
p 9.0e-13
N 47,745
Large GWAS
European

neutrophil count, basophil count

Allele A
OR 0.04
p 3.0e-10
N 170,143
Large GWAS
European

neutrophil count

Allele A
OR 0.04
p 6.0e-10
N 170,702
Large GWAS
European

granulocyte count

Allele A
OR 0.04
p 4.0e-9
N 169,822
Large GWAS
European

neutrophil count, eosinophil count

Allele A
OR 0.04
p 7.0e-9
N 170,384
Large GWAS
European

mosaic loss of chromosome Y measurement

Allele A
OR
β 0.057
p 4.0e-19
N 95,380
Large GWAS
East Asian

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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