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Retrieve a list of variants based on summary statistics from NIAGADS Genome-wide Association data.

Select an accession to view a listing of searchable datasets. Use the default cut-off of p-value ≤ 5 x 10-8 or specify your own threshold for genome-wide significance. For exome-array studies, we recommend a cut-off of p-value ≤ 1 x 10-3.

2016 Perelman School of Medicine, University of Pennsylvania. All rights reserved.

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  • Searches are sometimes 'redesigned' if database revisions lead to new parameters and/or new parameter choices.


  • When parameters have been modified and we cannot easily map your old choices into the new search, the search will be covered with a X. It means it needs to be revised.


  • Please open strategies marked with and click each search that needs revision.


  • genome annotations are constantly updated to reflect new biological information concerning the sequences.

  • when annotations are updated during a new release of our websites, some ids may change or be retired.
If your basket is in error, your basket contains old IDs that could not be mapped to new IDs.
  • download the basket valid IDs (tab delimited, clear all attributes) into a text file; you can later upload them into a new step
  • reset the basket by emptying it
Edit

Important!

  • You are saving/sharing this strategy, not the IDs in your result.
  • Results might change with subsequent releases of the site if the underlying data have changed.
  • To keep a copy of your current result, please download your IDs.
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Note: There is a 4,000 character limit.

Important!

  • You are saving/sharing this strategy, not the IDs in your result.
  • Results might change with subsequent releases of the site if the underlying data has changed.
  • To keep a copy of your current result, please download your IDs.
  • The following URL allows you to share your strategy with individuals. If you'd like to share
    your strategy with the entire community, visit the 'All' tab and click the 'Public' checkbox.
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