List of variants reported as uncertain significance for hematologic disorder by Institute of Human Genetics, Cologne University

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.2658G>C (p.Glu886Asp)	rs139002130	0.00055
NM_000064.4(C3):c.3537C>A (p.Asn1179Lys)	rs1918021723
NM_000186.4(CFH):c.1616G>T (p.Gly539Val)	rs1027258331
NM_139276.3(STAT3):c.1847A>G (p.Glu616Gly)	rs2144691780

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