rs10075801

This is a intron variant variant in the SLC22A4 gene.

GWAS Catalog Trait Associations (14)

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

leukocyte quantity

Allele G
OR 0.04
p 7.0e-26
N 172,435
Large GWAS
European

myeloid leukocyte count

Allele G
OR 0.04
p 5.0e-25
N 169,219
Large GWAS
European

granulocyte count

Allele G
OR 0.04
p 8.0e-23
N 169,822
Large GWAS
European

neutrophil count, eosinophil count

Allele G
OR 0.04
p 4.0e-22
N 170,384
Large GWAS
European

neutrophil count, basophil count

Allele G
OR 0.03
p 2.0e-16
N 170,143
Large GWAS
European

neutrophil count

Allele G
OR 0.03
p 8.0e-16
N 170,702
Large GWAS
European

citrate measurement

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele G
OR 0.02
p 3.0e-15
N 450,015
Large GWAS
multi-ancestry

dermatitis

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.04
p 8.0e-13
N 555,738
Major Consortium StudyLarge GWAS
multi-ancestry

diastolic blood pressure

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele A
OR 0.02
p 3.0e-11
N 609,354
Major Consortium StudyLarge GWAS
multi-ancestry

docosapentaenoate n3 DPA; 22:5n3 measurement

Allele A
OR 0.06
p 6.0e-9
N 14,296
Large GWAS
European

About SLC22A4

Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is an organic cation transporter and plasma integral membrane protein containing eleven putative transmembrane domains as well as a nucleotide-binding site motif. Transport by this protein is at least partially ATP-dependent. [provided by RefSeq, Jul 2008]

View all SLC22A4 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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