rs77046277

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 count

Allele C
OR
p 2.0e-200
N 643,370
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 0.41
p 9.0e-128
N 445,573
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 0.69
p 8.0e-115
N 408,112
Large GWAS
European
Allele C
OR 0.54
p 7.0e-25
N 171,643
Large GWAS
European

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 G
OR 0.60
p 2.0e-86
N 408,112
Large GWAS
European
Allele G
OR 0.40
p 6.0e-15
N 171,748
Large GWAS
European

neutrophil percentage of leukocytes

Allele G
OR 0.41
p 1.0e-52
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 0.45
p 1.0e-50
N 408,112
Large GWAS
European

hypothyroidism

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele G
OR 0.55
p 1.0e-8
N 583,911
Large GWAS
multi-ancestry

leukocyte quantity

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 0.12
p 9.0e-19
N 504,825
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 0.20
p 4.0e-11
N 408,112
Large GWAS
European
Allele C
OR 0.25
p 1.0e-35
N 153,950
Large GWAS
East Asian

myeloid leukocyte count

Allele G
OR 0.12
p 3.0e-11
N 151,807
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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