The NM_000552.5:c.4541T>G p.(Phe1514Cys) variant in VWF is a missense variant predicted to cause substitution of phenylalanine by cysteine at amino acid 1514. This variant is absent from gnomAD v4.1.0 (PM2_Supporting). The computational predictor REVEL gives a score of 0.93, which is above the ClinGen VWD VCEP threshold of >0.644 and predicts a damaging effect on VWF function (PP3). At least 1 proband with this variant displayed excessive mucocutaneous bleeding as well as laboratory phenotypes of very low VWF activity (measured by VWF:RCo), low activity/VWF:Ag ratio and loss of high molecular weight multimers, which together are highly specific for VWD type 2A. (PP4_moderate, PMID 8435341). The variant has been reported to segregate with VWD type 2A through >2 affected meioses from 1 family (PP1; PMID: 8435341). This variant has been reported in at least 1 additional proband with reduced VWF:Ag to activity ratio (PS4_supporting; PMID: 40393667). In summary, this variant meets the criteria to be classified as likely pathogenic for autosomal dominant von Willebrand disease Type 2A based on the ACMG/AMP criteria applied, as specified by the ClinGen VWD VCEP (v1): PP1, PP3, PP4_Moderate, PM2_Supporting, PS4_Supporting.