rs11666267

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GWAS Catalog Trait Associations (2)

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

level of T-cell leukemia/lymphoma protein 1A in blood

Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele A
OR 0.04
p 5.0e-17
N 47,745
Large GWAS
European

low affinity immunoglobulin epsilon Fc receptor measurement

Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele A
OR 0.04
p 1.0e-12
N 47,745
Large GWAS
European
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Research that mentions this SNP (1)

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Genetic association of ACSM1 variation with schizophrenia and major depressive disorder in the Han Chinese population
AssociationN=593Wenjin Li et al.(2015)· American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Exome sequencing study of 30 Brazilian ADHD trios identified 26 de novo SNVs, 134 very rare heterozygous variants, and 127 rare homozygous mutations across brain-expressed genes. Integration with 503 Brazilian controls and public ADHD databases revealed genes in glutamatergic and serotonergic synaptic pathways, cell adhesion, and synapse-related biological functions as significantly enriched in ADHD.

Traits studied:Attention-Deficit/Hyperactivity Disorder (ADHD)
PubMedDOIMetascience Observatory

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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