List of variants reported as uncertain significance for Glanzmann thrombasthenia 1 by ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000212.3(ITGB3):c.2311C>T (p.Pro771Ser)	rs766423016	0.00001
NM_000419.5(ITGA2B):c.2417G>A (p.Ser806Asn)	rs1189791675	0.00001
NM_000212.3(ITGB3):c.2216_2217insAGCA (p.Ile740fs)	rs2143150604
NM_000419.5(ITGA2B):c.1210+609C>T
NM_000419.5(ITGA2B):c.1375G>A (p.Asp459Asn)
NM_000419.5(ITGA2B):c.1440-13_1440-1del	rs2048585829
NM_000419.5(ITGA2B):c.205G>A (p.Gly69Ser)
NM_000419.5(ITGA2B):c.2150T>C (p.Leu717Pro)	rs2143447451
NM_000419.5(ITGA2B):c.337C>T (p.Gln113Ter)
NM_000419.5(ITGA2B):c.533G>C (p.Arg178Pro)
NM_000419.5(ITGA2B):c.59T>G (p.Leu20Arg)
NM_000419.5(ITGA2B):c.886G>A (p.Gly296Arg)	rs753264426

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