rs184409696

This is a regulatory region variant variant in the EHD3 gene.

GWAS Catalog Trait Associations (4)

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

monocyte count

Allele G
OR 0.14
p 4.0e-31
N 521,594
Large GWAS
European
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 0.14
p 2.0e-21
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 G
OR 0.14
p 4.0e-23
N 408,112
Large GWAS
European
Allele G
OR 0.12
p 2.0e-24
N 394,642
Large GWAS
European

leukocyte quantity

Vuckovic D et al. The Polygenic and Monogenic Basis of Blood Traits and Diseases. Cell 182(5):1214-1231.e11 (2020)
Allele C
OR 0.10
p 1.0e-13
N 408,112
Large GWAS
European
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 0.09
p 9.0e-9
N 504,825
Large GWAS
multi-ancestry

neutrophil 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 0.09
p 2.0e-10
N 408,112
Large GWAS
European

myeloid leukocyte count

Allele G
OR
p 5.0e-13
N 746,667
Large GWAS
multi-ancestry

About EHD3

Predicted to enable nucleic acid binding activity. Involved in several processes, including cytosolic transport; endocytic recycling; and protein homooligomerization. Acts upstream of or within protein localization to plasma membrane and regulation of cardiac muscle cell membrane potential. Located in ciliary pocket membrane and recycling endosome membrane. [provided by Alliance of Genome Resources, Jul 2025]

View all EHD3 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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