rs1456896

This is a intergenic variant variant.

GWAS Catalog Trait Associations (5)

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

neutrophil count

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.02
p 3.0e-25
N 432,666
Large GWAS
multi-ancestry

myeloid leukocyte count

Allele T
OR
p 2.0e-18
N 746,667
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 T
OR 0.02
p 2.0e-16
N 504,825
Large GWAS
multi-ancestry

inflammatory bowel disease

Allele T
OR 1.09
p 7.0e-15
N 34,366
Large GWAS
European
Allele T
OR 1.08
p 3.0e-13
N 34,652
Large GWAS
multi-ancestry

Crohn's disease

Allele T
OR 1.10
p 1.0e-13
N 20,883
Large GWAS
multi-ancestry
Allele T
OR 1.14
p 1.0e-8
N 21,389
Meta-analysisLarge 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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