Supplementary Table S1 & S2 Proband and Variant Information:
Case2: GT3, Female, 32, French
DiseaseAssertion: Glanzmann thrombasthenia
FamilyInfo: N/A
ParentalGenotype: N/A
CasePresentingHPOs: HP:0000421, HP:0031364, HP:0000979, HP:0002239
(Epistaxis, ecchymosis, purpura, GI bleeding,)
CaseHPOFreeText: Excessive menstrual bleeding, proband sometimes hospitalized with severe symptoms
CaseNotHPOs: N/A
CaseNotHPOsFreeText: N/A
ProteinExpression: Flow cytometry showed <5% expression of αIIbβ3 (See Supplementary Table 1)
PlateletAggregation: Absent platelet aggregation (See Supplementary Table 1)
CasePreviousTesting: Sanger sequencing of ITGA2B and ITGB3
Gene: ITGB3
Variant: NM_000212.2:c.353T>A, NM_000212.2:c.709_710del, NM_000212.2:c.1732G>A
LegacyVariant: N/A
ClinVar: N/A
CAiD: CA291224511, CA8623029 and CA8623343
gnomAD: MAF in the European non Finnish populationis 0.00001796 http://gnomad.broadinstitute.org/variant/17-45363717-CAG-C and MAF in the Other popualation is 0.0008149 http://gnomad.broadinstitute.org/variant/17-45376715-G-A