The NM_000552.5:c.3569G>A variant in VWF is a missense variant predicted to cause substitution of cysteine by tyrosine at amino acid 1190 (p.Cys1190Tyr). At least 1 patient with this variant displayed excessive mucocutaneous bleeding as well as laboratory phenotypes of very low VWF activity, low activity/VWF:Ag ratio, and loss of high molecular weight multimers, which together are highly specific for VWD type 2A. (PP4_moderate, PMID 34532631). Additional consistent phenotypes were also reported in the patient, specifically, FVIII activity consistent with VWF antigen. This variant has been reported in 5 additional probands meeting PP4 laboratory phenotype criteria (PS4; PMID 20351307, 32864553, 32803740, 34355501). Another missense variant NM_000552.5:c.3568T>C (p.Cys1190Arg) in the same codon has been classified as pathogenic for VWD type 2A by the ClinGen VWD VCEP (PM5). The Grpmax filtering allele frequency in gnomAD v4.1 is 0.0000006195 (1/1180046 European non-Finnish population), which is lower than the ClinGen VWD VCEP threshold of <0.0001 for type 2A (PM2_Supporting). The computational predictor REVEL gives a score of 0.947, which is above the ClinGen VWD VCEP threshold of >0.644 and predicts a damaging effect on VWF function (PP3). In summary, this variant meets the criteria to be classified as pathogenic for autosomal dominant VWF type 2A based on the ACMG/AMP criteria applied, as specified by the ClinGen VWD VCEP: PP4_Moderate, PS4, PM5, PM2_Supporting, PP3. (ClinGen von Willebrand Disease Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for VWF Version 1.0.0)