rs2773822

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GWAS Catalog Trait Associations (1)

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

E-selectin amount

Loya H et al. “A scalable variational inference approach for increased mixed-model association power.” Nature Genetics 57(2):461-468 (2025)
Allele T
OR 0.03
p 1.0e-14
N 47,745
Large GWAS
European
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Research that mentions this SNP (1)

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Genome‐wide association study in German patients with attention deficit/hyperactivity disorder
AssociationN=1,795Anke Hinney et al.(2011)· American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

A genome-wide association study in 495 German ADHD patients and 1,300 population-based controls identified 30 independent SNPs with p-values below 7.57×10^-5 for replication testing. The best SNP (rs2556378 in BCL11A, p=8.38×10^-7, OR=1.61) and second-best SNP (rs5016282 in GRM5, p=1.78×10^-6, OR=1.85) showed directionally consistent effects in replication families (n=320) and meta-analysis, but no genome-wide significant results (p<5×10^-8) were achieved despite high ADHD heritability.

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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