rs61744929

GWAS Catalog Trait Associations (12)

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

neutrophil count

Allele C
OR 0.06
p 3.0e-17
N 519,288
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 C
OR 0.05
p 8.0e-11
N 408,112
Large GWAS
European
Allele C
OR 0.05
p 7.0e-12
N 394,642
Large GWAS
European

placenta growth factor measurement

Allele C
OR 0.14
p 7.0e-16
N 47,745
Large GWAS
European

reticulocyte count

Allele C
OR 0.05
p 9.0e-15
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 C
OR 0.06
p 1.0e-11
N 408,112
Large GWAS
European

mean corpuscular hemoglobin concentration

Allele C
OR 0.05
p 8.0e-13
N 491,553
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 C
OR 0.05
p 5.0e-11
N 408,112
Large GWAS
European

lymphocyte percentage of leukocytes

Allele C
OR 0.05
p 1.0e-12
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 C
OR 0.06
p 5.0e-12
N 408,112
Large GWAS
European

reticulocyte amount

Allele C
OR 0.05
p 2.0e-12
N 394,642
Large GWAS
European

monocyte count

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 1.0e-11
N 408,112
Large GWAS
European

hemoglobin measurement

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.05
p 3.0e-10
N 408,112
Large GWAS
European
Allele C
OR
β 0.047
p 2.0e-8
N 684,122
Large GWAS
European

body composition measurement

Allele C
OR 0.16
p 4.0e-10
N 39,144
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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