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. Author manuscript; available in PMC: 2022 Mar 1.
Published in final edited form as: Genet Med. 2021 May 11;23(9):1689–1696. doi: 10.1038/s41436-021-01193-y

Fig. 2. Molecular diagnoses (probands only) made by clinical genome sequencing (cGS) and standard-of-care (SOC).

Fig. 2

*A participant with multiple diagnoses is represented by more than one column. P/LP pathogenic/likely pathogenic, VUS variant of uncertain significance.