The c.167T>C variant in GP9 is a missense variant predicted to cause substitution of Leucine by Proline at amino acid 56 (p.Leu56Pro). At least one patient (Patient II-2 in PMID: 9886312) with this variant had aggregation absent for ristocetin and present for all other agonists as well as less than 10% expression of GP9 measured by flow cytometry, 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 PM3 points, PM3_Supporting). The variant has been reported to segregate in the proband plus 1 additional homozygous BSS affected family member (1 PP1 point, PP1). The computational predictor REVEL gives a score of 0.849, which is above the ClinGen PD VCEP threshold of >0.773 and predicts a damaging effect on function (PP3_Moderate). The largest MAF allele frequency in gnomAD v4.1.0 is 0.000001695 (based on 2/1179872 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: PP4, PM3_Supporting, PP1, PP3_Moderate and PM2_Supporting (VCEP specifications version 1.1).