metadata
license: cc-by-4.0
task_categories:
- tabular-regression
- tabular-classification
tags:
- gwas
- summary-statistics
- psychiatric-genomics
- pgc
- sud
- mental-health
- genetics
- genomics
- biology
- health
- bioinformatics
pretty_name: PGC Substance Use Disorders GWAS Summary Statistics
size_categories:
- 1M-10M
configs:
- config_name: SUD2023
default: true
data_files:
- split: train
path: data/SUD2023/*.parquet
- config_name: sud2018-alc
data_files:
- split: train
path: data/sud2018-alc/*.parquet
- config_name: sud2019-alcuse
data_files:
- split: train
path: data/sud2019-alcuse/*.parquet
- config_name: sud2020-cud
data_files:
- split: train
path: data/sud2020-cud/*.parquet
- config_name: sud2020-op
data_files:
- split: train
path: data/sud2020-op/*.parquet
language:
- en
source_datasets:
- pgc
PGC Substance Use Disorders — GWAS Summary Statistics
Dataset Description
Genome-wide association study (GWAS) summary statistics for Substance Use Disorders phenotypes from the Psychiatric Genomics Consortium (PGC).
This dataset contains multiple GWAS publications as separate subsets (configs). Each can be loaded independently.
Usage
from datasets import load_dataset
# Load a specific GWAS (e.g., SUD2023)
ds = load_dataset("OpenMed/pgc-substance-use", "SUD2023")
print(ds)
Available Configs
from datasets import get_dataset_config_names
configs = get_dataset_config_names("OpenMed/pgc-substance-use")
print(configs)
Subsets (Publications)
| Config | Phenotype | Journal | Year | PubMed | Rows | License |
|---|---|---|---|---|---|---|
SUD2023 |
Substance Use Disorder | Nature Mental Health | 2023 | 37250466 | 5,736,488 | CC BY 4.0 |
sud2018-alc |
Alcohol Dependence | Nature Neuroscience | 2018 | 30482948 | — | CC BY 4.0 |
sud2019-alcuse |
Alcohol Use / AUDIT | American Journal of Psychiatry | 2019 | 30336701 | — | CC BY 4.0 |
sud2020-cud |
Cannabis Use Disorder | Lancet Psychiatry | 2020 | 33096046 | — | CC BY 4.0 |
sud2020-op |
Opioid Dependence | Molecular Psychiatry | 2020 | 32099098 | 57,445,238 | CC BY 4.0 |
Data Format
All data has been converted to Apache Parquet format with shards of 10,000 rows. Common columns include:
| Column | Description |
|---|---|
SNP / ID |
SNP rsID or variant identifier |
CHR |
Chromosome |
BP / POS |
Base-pair position (typically GRCh37/hg19) |
A1 / ALT |
Effect allele |
A2 / REF |
Non-effect (reference) allele |
OR / BETA |
Odds ratio or effect size |
SE |
Standard error |
P |
P-value |
INFO |
Imputation quality score |
FRQ / MAF |
Allele frequency |
_source_file |
Original source filename |
Note: Column names vary between publications. The
_source_filecolumn tracks the original file each row came from.
Citation
When using any subset, please cite:
- The original publication (see PubMed links above)
- The data DOI from Figshare (see supplementary metadata)
- Acknowledge the PGC:
"Data were obtained from the Psychiatric Genomics Consortium — https://pgc.unc.edu/"
Terms of Use
This dataset is released under the CC BY 4.0 license.
By using PGC summary statistics you agree to:
- Cite the original publication(s)
- Not attempt to re-identify individual participants
- Comply with the PGC's data use policies
Source
- Consortium: Psychiatric Genomics Consortium (PGC)
- PGC Downloads: pgc.unc.edu/for-researchers/download-results/
Last updated: April 2026