The NM_000212.3(ITGB3):c.812dup variant is a frameshift variant in exon 6 predicted to cause a premature stop codon in exon 6/15 leading to nonsense mediated decay in a gene in which loss-of-function is an established disease mechanism (PVS1). At least one patient (Patient 12 in PMID:15748237) with this variant displayed mucocutaneous bleeding and impaired aggregation with all agonists except ristocetin, which is highly specific for Glanzmann thrombasthenia (PP4_moderate). Additionally, αIIbβ3 surface expression was reduced to 0%, as measured by flow cytometry. Patient 12 (PMID:15748237) is homozygous for this variant (0.5pt; PM3_Supporting). The variant is absent from gnomAD, PM2_Supporting). In summary, this variant meets the criteria to be classified as Pathogenic for autosomal recessive Glanzmann Thrombasthenia based on the ACMG/AMP criteria applied, as specified by the ClinGen PD VCEP: PVS1, PP4_Moderate, PM2_Supporting, PM3_Supporting (VCEP specifications version 2.1).