List of variants reported as uncertain significance for hematologic disorder by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001355436.2(SPTB):c.2519G>A (p.Arg840His)	rs146326769	0.00065
NM_000312.4(PROC):c.113G>A (p.Arg38Gln)	rs773107370	0.00010
NM_000064.4(C3):c.1125C>A (p.Phe375Leu)
NM_001142864.4(PIEZO1):c.2165C>T (p.Pro722Leu)
NM_001360016.2(G6PD):c.859G>A (p.Glu287Lys)	rs387906471

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