This PheWeb portal provides interactive access to genome-wide association study results from 206,159 Estonian Biobank participants, covering 5,491 ICD-10-based disease endpoints and approximately 18.8 million genetic variants linked to nationwide longitudinal health records.
The results presented here form part of the work described in our medRxiv preprint, available at https://www.medrxiv.org/content/10.1101/2025.03.18.25324091v2, which provides the scientific context, methodological details and interpretation underlying these results. We kindly ask users of this resource to consult and cite the preprint when referring to findings presented on this portal. For questions or enquiries regarding the resource, please contact Priit Palta at priit.palta@ut.ee.