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. Author manuscript; available in PMC: 2020 Dec 1.
Published in final edited form as: J Genet Couns. 2019 Sep 3;28(6):1107–1118. doi: 10.1002/jgc4.1161

Figure 3. Variant types reported for patients with non-diagnostic WES.

Figure 3.

15/43 (35%) had a pathogenic variant reported, 19/43 (44%) of patients without a pathogenic or likely pathogenic variant reported at least one VUS in a gene related to the patient’s clinical phenotype, and 9/43 (21%) only had a research variant.