The NM_000552.5:c.2637C>A variant in VWF is a missense variant predicted to cause substitution of aspartate by glutamate at amino acid 879 (p.Asp879Glu). At least 1 patient with this variant displayed excessive mucocutaneous bleeding as well as low FVIII activity and decreased VWF:FVIII binding, which is highly specific for VWD type 2N. (PP4_moderate, PMID 26988807). Additional consistent phenotypes were also reported in the patient including normal VWF:Ag, and normal HMW multimers. This variant has been detected in 1 individual with von Willebrand Disease type 2N. The individual is compound heterozygous for the variant and a pathogenic variant as determined by the ClinGen VWD VCEP, confirmed in trans by the authors (p.Arg854Gln) (PM3, PMID 26988807). This variant is absent from gnomAD v4.1 (PM2_Supporting). Another missense variant c.2635G>A, p.Asp879Asn (PMIDs 9845532, 34298581) in the same codon has been classified as pathogenic for VWD type 2N by the ClinGen VWD VCEP (PM5). Splicing prediction using SpliceAI revealed no expected effects on splicing due to any of these variants. In summary, this variant meets the criteria to be classified as a variant of likely pathogenic for von Willebrand Disease type 2N based on the ACMG/AMP criteria applied, as specified by the ClinGen VWD VCEP: PP4_Moderate, PM3, PM2_Supporting, and PM5. (ClinGen VWD VCEP, VWD type 2N rule specifications v1.0.0; date of approval)