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. 2022 Apr 27;13:866169. doi: 10.3389/fgene.2022.866169

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Copyright © 2022 Elhanan, Kiser, Neveux, Dabe, Bolze, Metcalf, Lu and Grzymski.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Bar graph depicting counts of participants who meet increasingly restrictive criteria. From bottom to top, participants are limited to (1) those who had a positive finding for HBOC, LS, and/or FH; (2) those who were also notified of their finding and had a genetic consultation; (3) those who also had an EHR record at Renown; (4) those who also had no knowledge of their finding documented in their EHR prior to notification; (5) those who also had a relevant genetic diagnosis documented in their EHR after notification; (6) those whose diagnosis was specific to their condition; and (7) those whose diagnosis appeared in their problem list. Total participant counts for each additional criterion appear on the x-axis, while counts for each distinct condition (or set of conditions) are superimposed on each bar.