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Variation Report page for variant NM_000138.4(FBN1):c.4786C>T (p.Arg1596Ter). The Variation Report page displays aggregate information regarding the variant review status (A), interpretation (B), alternative variant expressions (C), and impacted gene(s) (D). Assertions and evidence provided by each submitter are displayed in the Clinical assertions, Summary evidence, and Supporting observations tables at the bottom of the page (F).
