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. 2021 Sep 13;141(3-4):495–504. doi: 10.1007/s00439-021-02338-4

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 3 — Variant distribution. A. Mean number of variants identified per child across race/ethnicity groups with reported p-value of ANOVA for mean number of variants vs dichotomized race/ethnicity (White/Asian and Black/Hispanic). B. Known Variant rate. Left: Distribution of Known Variants across race/ethnicity groups. Known Variant rate was compared by ANOVA between dichotomized race/ethnicity groups (White/Asian and Black/Hispanic). Right: Distribution of Known Variants across characteristics is shown. Color scheme is as described in Fig 2. C. Predicted deleterious VUS rate. Left: Distribution of predicted deleterious VUSs (by PROVEAN prediction) across race/ethnicity groups. Deleterious VUS rate was compared by ANOVA between dichotomized race/ethnicity groups (White/Asian and Black/Hispanic). Right: Distribution of deleterious VUSs across characteristics is shown. Color scheme is as described in Fig 2