rs1892548

GWAS Catalog Trait Associations (7)

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

monocyte count

Allele C
OR
p 5.0e-234
N 639,696
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 6.0e-114
N 444,975
Large GWAS
multi-ancestry
Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.06
p 5.0e-165
N 408,112
Large GWAS
European
Allele C
OR 0.05
p 2.0e-156
N 394,642
Large GWAS
European
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele C
OR 0.08
p 1.0e-125
N 259,608
Major Consortium StudyLarge GWAS
European
Kachuri L et al. Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. American Journal of Human Genetics 108(10):1823-1835 (2021)
Allele C
OR
p 8.0e-60
N 234,690
Large GWAS
European
Allele C
OR 0.06
p 7.0e-63
N 170,721
Large GWAS
European

monocyte 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 C
OR 0.06
p 6.0e-161
N 408,112
Large GWAS
European
Allele C
OR 0.05
p 1.0e-159
N 394,642
Large GWAS
European
Allele C
OR 0.06
p 3.0e-64
N 170,494
Large GWAS
European

granulocyte percentage of myeloid white cells

Allele C
OR 0.06
p 3.0e-54
N 169,545
Large GWAS
European

lymphocyte:monocyte ratio

Kachuri L et al. Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. American Journal of Human Genetics 108(10):1823-1835 (2021)
Allele T
OR
p 8.0e-52
N 234,184
Large GWAS
European

C-C motif chemokine 24 measurement

Allele C
OR 0.03
p 3.0e-14
N 47,745
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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