Skip to main content

Division of Genomic Medicine

A Catalog of Published Genome-Wide Association Studies

Update (5/12/15): The NHGRI-EBI GWAS Catalog has moved to the European Molecular Biology Laboratory-European Bioinformatics Institute (EMBL-EBI) at Users may now find the new search interface and updated content at this site.  Questions about the GWAS Catalog may be directed to

Why has the catalog moved to EMBL-EBI?
From September 2010 to the present, delivery and development of the Catalog has been a collaborative project between EMBL-EBI and NHGRI. In March 2015 the Catalog infrastructure moved to EMBL-EBI to enable delivery of an improved user interface, including ontology driven Catalog searching, and new curatorial infrastructure, supporting improved QC processes. Catalog content available through this original GWAS Catalog website was last updated on February 20th 2015 with all previous and updated content available at EMBL-EBI. 

The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog).
Read our recent article from Nucleic Acids Research.

Published Genome-Wide Associations
Credit: Darryl Leja and Teri Manolio, NHGRI; Tony Burdett, Dani Welter, and Helen Parkinson, EBI

An archived tab-delimited file of the GWAS Catalog content prior to the EBI transition is available here: Tab Delimited File

The genome-wide association study (GWAS) publications in the Catalog include a primary GWAS analysis, defined as array-based genotyping and analysis of 100,000+ pre-QC SNPs selected to tag variation across the genome and without regard to gene content.  GWAS data from published studies which are incorporated into new GWAS analyses are eligible, provided they meet the other criteria.  Studies imputing sequencing data to genotyping arrays are eligible as long as the arrays include sufficient genome-wide coverage so that the post-imputation analysis meets the definition of a GWAS analysis, as described above. The scope of the GWAS Catalog is currently being expanded to include studies of large-scale targeted/non-genome-wide arrays, including the Metabochip, Immunochip and Exome arrays. This is currently in a pilot phase where prioritization of targeted and exome array studies for inclusion in the Catalog is by 1) relevance of the trait analyzed 2) user request.  

How to cite the NHGRI GWAS Catalog:
MacArthur J, Bowler E, Cerezo M, Gil L, Hall P, Hastings E, Junkins H, McMahon A, Milano A, Morales J, Pendlington Z, Welter D, Burdett T, Hindorff L, Flicek P, Cunningham F, and Parkinson H. The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). Nucleic Acids Research, 2017, Vol. 45 (Database issue): D896-D901.

For questions or comments about this page, send an e-mail to:





Notice: The updated Catalog content may now be searched at

An archived, tab-delimited file of the GWAS Catalog content prior to the EBI transition is available here: Tab Delimited File

Date Added to Catalog (since 11/25/08) First Author/Date/ Journal/Study Disease/Trait Initial
Sample Description
Replication Sample Description Region Reported Gene(s) Mapped Gene(s) Strongest SNP-Risk Allele Context Risk Allele Frequency in Controls P-value
OR or beta-coefficient and [95% CI]
[SNPs passing QC]
11/12/14 Barnett GC
April 28, 2014
Radiother Oncol
A genome wide association study (GWAS) providing evidence of an association between common genetic variants and late radiotherapy toxicity.
Response to radiotherapy in cancer (late toxicity) 579 European ancestry prostate cancer cases, 1,194 European ancestry breast cancer cases 516 European ancestry prostate cancer cases, 862 prostate cancer cases, 355 breast cancer cases 15q21.1 SEMA6D SQRDL - SEMA6D rs16958536-? 0.22 4 x 10-6 (Breast cancer, telangiectasia, multivariable analysis) 1.66 Illumina
[2,417,493] (imputed)
02/06/14 Wojczynski MK
July 19, 2013
BMC Med Genet
Genetics of coronary artery calcification among African Americans, a meta-analysis.
Coronary artery calcification 5,823 African American individuals 9,992 European ancestry individuals 15q21.1 SEMA6D SEMA6D rs8028579-T intron 0.11 7 x 10-6 (AA) .3 [0.16-0.44] unit increase Affymetrix & Illumina
[up to 2,727,966] (imputed)
10/23/12 Boraska V
August 22, 2012
Am J Med Genet B Neuropsychiatr Genet
Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.
Eating disorders Up to 2,567 European ancestry individuals Up to 767 European ancestry cases, up to 486 European ancestry controls 15q21.1 SEMA6D SEMA6D rs1898111-A intron 0.837 8 x 10-6 (OCPD) 1.15 [1.08-1.22] Illumina

Top of page

Catalog Data Last Updated: February 20, 2015
Web Page Text Last Updated: September 16, 2015