The NM_00138 c.3632_3634del is an in-frame deletion in FBN1predicted to cause a deletion of a phenylalanine at position 1211 (p.Phe1211del). This variant was found in a proband with a clinical diagnosis of Marfan syndrome (internal data, University of Ghent) (PP4). This variant was also found in a proband with ectopia lentis and an adverse aortic event and was found to segregate with the disease in two affected family members (internal data, University of Tokyo) (PP1). It has been reported in the literature in two unrelated individuals with ectopia lentis (PMID 19159394, 16222657), in one individual with a clinical diagnosis of Marfan syndrome (Ambry Genetics ClinVarentry) and in two unrelated individuals with thoracic aortic aneurysm and/or dissection (PMID 37042257, 33059708) (PS4). This variant is not present in gnomAD(PM2_sup; https://gnomad.broadinstitute.org/). This variant is located in a non-repeat region in a cbEGF-like domain of the protein (PM4). The variant in FBN1 has been reported three times in ClinVar as likely pathogenic (Variation ID: 549178). In summary, this variant meets criteria to be classified as likely pathogenic for Marfan syndrome based on the ACMG/AMP criteria applied, as specified by the ClinGen FBN1 VCEP: PS4, PM4, PM2_Sup, PP1, PP4.