rs191674933

This is a upstream gene variant variant in the ACTRT3 gene.

GWAS Catalog Trait Associations (7)

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

eosinophil percentage of leukocytes

Allele T
OR 0.03
p 3.0e-30
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 T
OR 0.03
p 6.0e-22
N 408,112
Large GWAS
European

eosinophil count

Allele T
OR 0.02
p 4.0e-25
N 474,237
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 T
OR 0.02
p 1.0e-21
N 408,112
Large GWAS
European
Allele T
OR 0.02
p 2.0e-17
N 394,642
Large GWAS
European

erythrocyte volume

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 0.03
p 4.0e-17
N 583,965
Major Consortium StudyLarge GWAS
multi-ancestry

chromosome, telomeric region length

Allele A
OR 0.02
p 4.0e-15
N 438,351
Major Consortium StudyLarge GWAS
European

lung adenocarcinoma

Allele A
OR 1.11
p 2.0e-12
N 143,595
Large GWAS
multi-ancestry

respiratory system disease

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 0.17
p 2.0e-12
N 447,762
Major Consortium StudyLarge GWAS
European

Epidermal Inclusion Cyst

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 0.06
p 4.0e-12
N 420,570
Major Consortium StudyLarge GWAS
European

About ACTRT3

Predicted to be located in cytoplasm; cytoskeleton; and male germ cell nucleus. Predicted to be active in actin cytoskeleton. [provided by Alliance of Genome Resources, Jul 2025]

View all ACTRT3 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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