rs10849448

GWAS Catalog Trait Associations (22)

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

monocyte percentage of leukocytes

Allele G
OR 0.05
p 4.0e-134
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 G
OR 0.06
p 1.0e-122
N 408,112
Large GWAS
European
Allele G
OR 0.06
p 4.0e-46
N 170,494
Large GWAS
European

granulocyte percentage of myeloid white cells

Allele G
OR 0.05
p 7.0e-27
N 169,545
Large GWAS
European

platelet crit

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele G
OR 0.03
p 1.0e-25
N 408,112
Large GWAS
European

disorder of pharynx

Allele G
OR 0.90
p 2.0e-22
N 232,365
Large GWAS
European

eosinophil percentage of leukocytes

Allele G
OR 0.02
p 2.0e-18
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 G
OR 0.02
p 5.0e-16
N 408,112
Large GWAS
European

aspartate aminotransferase measurement

Allele A
OR 0.02
p 6.0e-16
N 928,679
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 A
OR 0.01
p 5.0e-10
N 493,058
Large GWAS
multi-ancestry
Allele A
OR 6.09
p 1.0e-9
N 389,565
Large GWAS
multi-ancestry

serpin A9 measurement

Allele G
OR 0.05
p 3.0e-15
N 47,745
Large GWAS
European

C-X-C motif chemokine 13 measurement

Allele G
OR 0.05
p 6.0e-15
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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