The c.89G>A (p.Cys30Tyr) variant in GP1BB is a missense variant predicted to cause substitution of Cysteine by Tyrosine at amino acid 30 (p.Cys30Tyr). At least one patient (Proband PMID: 12958615) with this variant had aggregation absent for ristocetin and present for all other agonists as well as less than 10% expression of GPIba and GP1bb measured by Western blot, which is highly specific for Bernard-Soulier syndrome. Additionally, the patient had excessive mucocutaneous bleeding and macrothrombocytopenia which are consistent with Bernard-Soulier syndrome (PP4). This individual was homozygous for the variant (0.5 points, PM3_Supporting). The variant has been reported to segregate in the proband plus 1 additional homozygous BSS affected sibling (1 point, PP1). Surface expression of the GPIba measured by flow cytometry in CHO cells transiently co-transfected with p.Cys30Tyr variant GP1b and wild type GP1a and GP9 showed absent expression, indicating that this variant impacts protein function (PMID: 12958615)(PS3_supporting). The computational predictor REVEL gives a score of 0.792, which is above the ClinGen PD VCEP threshold of >0.773 and predicts a damaging effect on GP1BB function (PP3_Moderate). This variant is absent from gnomAD v4.1.0 (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: PP3_Moderate, PP1, PP4, PM2_Supporting, PM3_Supporting and PS3_Supporting (VCEP specifications version 1.1).