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. 2019 Jun 4;21(12):2676–2680. doi: 10.1038/s41436-019-0558-2

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — Reporting of race in genome/exome sequencing (GS/ES) studies. a The percent of studies reporting age, gender, race, and ethnicity as a demographic variable. b The number of patients included in all studies as identified by race. c,d The number of c White and d Black patients with published sequencing data. The number of patients with existing data is shown in dark blue and the number of additional patients needed to sequence to reach 90% power to detect a pathogenic variant present in 10% of patients is shown in light blue. NHL non-Hodgkin lymphoma.