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

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_015175.3(NBEAL2):c.4361C>T (p.Thr1454Met)	rs371607035	0.00003
NM_015175.3(NBEAL2):c.6631G>A (p.Asp2211Asn)	rs781499875	0.00002
NM_015175.3(NBEAL2):c.4085G>A (p.Arg1362Gln)	rs781185845	0.00001
NM_015175.3(NBEAL2):c.2044A>T (p.Ile682Phe)	rs773164015
NM_015175.3(NBEAL2):c.3907C>A (p.Pro1303Thr)	rs769255839
NM_015175.3(NBEAL2):c.8164-1G>A	rs2107465570

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