Psychiatric Genomics Consortium ADHD GWAS Summary Statistics

PGC Attention Deficit Hyperactivity Disorder GWAS Summary Statistics contain genome-wide association study results for ADHD phenotypes. The dataset is organized by publication, with each available as a separate subset. It was created by OpenMed and last updated in April 2026.

Use Cases

• Identify significant genetic variants from p-values and effect sizes for ADHD risk.
• Perform fine-mapping of ADHD-associated loci using chromosome and base-pair position data.
• Calculate polygenic risk scores by aggregating effect estimates across single nucleotide polymorphisms.
• Conduct cross-trait genetic correlation analyses using summary statistics from different PGC publications.
• Replicate findings from specific studies like 'adhd2010' by loading individual publication subsets.

Strengths

• Data originates from the authoritative Psychiatric Genomics Consortium.
• Multiple independent GWAS publications are available as separate, loadable subsets.

Limitations

• The specific number of samples, variants, or summary statistic rows is unknown.
• Geographic and ancestral diversity of the underlying cohorts is unspecified.

Provenance

Source

Psychiatric Genomics Consortium (PGC).

Collection Method

Genome-wide association study meta-analysis.

Time Range

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Freshness

Last updated in April 2026.

Geography

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