The NM_000138 c.2669G>A variant is a missense variant in FBN1 predicted to cause a substitution of cysteine by tyrosine at amino acid position 890. This variant has not been reported in the literature but was identified at one institution as de novo in proband with ectopia lentis and a systemic score of 2 (PP4, PM6; UZG). This variant has also been reported four times in ClinVar, with two classifications of likely pathogenic and two classifications of pathogenic (Variation ID: 431935). It is not present in gnomAD v2.1.1 or 3.1.2 (PM2_supporting; https://gnomad.broadinstitute.org/). This variant affects a cysteine residue in the hybrid 2 domain; cysteine residues in the hybrid domains are believed to be important for proper protein folding (PM1). Computational prediction tools and conservation analysis support that this variant may impact the protein (PP3; REVEL = 0.926). The constraint z-score for missense variants affecting FBN1 is 5.06 (PP2). Three other missense variants at the same amino acid position (p.Cys890Arg, p.Cys890Gly, p.Cys890Trp) have been identified and are classified as likely pathogenic (PM5; PMIDs: 12938084, 16222657, 20564469). 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: PM1, PM5, PM6, PM2_supporting, PP2, PP3, PP4.