The c.442dup (p.Val148GlyfsTer67) variant in GP9 is a frameshift variant that may cause a premature stop codon that is predicted to escape nonsense mediated decay, however the truncation includes the functionally important transmembrane domain (alters amino acids 148-169) in a gene where loss-of-function is an established disease mechanism (PVS1_Strong). At least one patient (Patient P13 in PMID: 21173099) with this variant had aggregation absent for ristocetin and present for all other agonists as well as less than 10% expression of GPIba and GP9 measured by flow cytometry, which is highly specific for Bernard-Soulier syndrome. Additionally, the patient had excessive mucocutaneous bleeding is consistent with Bernard-Soulier syndrome (PP4). This individual was homozygous for the variant (0.5 PM3 points, PM3_Supporting). The Grpmax Filtering allele frequency in gnomAD v4.1.0 is 0.0000003000 (based on 2/1165574 alleles) in the European (non-Finnish) population, which is lower than the ClinGen PD VCEP threshold (<0.0000329; PM2_Supporting). In summary, this variant meets the criteria to be classified as Likely Pathogenic for autosomal recessive Bernard-Soulier syndrome based on the ACMG/AMP criteria applied, as specified by the ClinGen PD VCEP: PVS1_Strong, PP4, PM3_Supporting and PM2_Supporting (VCEP specifications version 1).