The NM_00138 c.3554G>A is a missense variant in FBN1 predicted to cause a substitution of a glycine by aspartic acid at amino acid 1185 (p.Gly1185Asp), in a cbEGF-like domain of the protein. This variant was found in a proband who met revised Ghent criteria with a clinical diagnosis of Marfan syndrome (MFS) (PMID 35058154, internal lab data, PP4). This variant has been reported three times in ClinVar: once as pathogenic, once as likely pathogenic, and once as uncertain significance (Variation ID: 549173). This variant was also found to be de novo in a proband with infantile MFS without confirmation of paternity and maternity (PM6, PS4_Sup; internal lab data). This variant is not present in gnomAD (PM2_sup; https://gnomad.broadinstitute.org/ v2.1.1). Computational prediction tools and conservation analysis suggest that this variant may impact the protein (REVEL: 0.942, PP3). The constraint z-score for missense variants affecting FBN1 is 5.06 (PP2). 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: PM6, PS4_Sup, PM2_Sup, PP2, PP3, PP4.