@misc{indiciaeebdd2ebeee09,
  title = {Surveying the contribution of rare variants to the genetic architecture of human disease through exome sequencing of 177,882 UK Biobank participants},
  author = {Wang, Q. and Dhindsa, R. S. and Carss, K. and Harper, A. R. and Nag, A. and Tachmazidou, I. and Vitsios, D. and Deevi, S. V. and Mackay, A. and Muthas, D. and Hühn, M. and Monkley, S. and Olsson, H. and Wasilewski, S. and Smith, K. R. and March, R. and Platt, A. and Haefliger, C. and AstraZeneca Genomics Initiative, and Petrovski, S.},
  year = {2020},
  doi = {10.1101/2020.12.13.422582},
  url = {https://www.biorxiv.org/content/10.1101/2020.12.13.422582v1},
  note = {Source identifier: 10.1101/2020.12.13.422582}
}