List of variants reported as likely pathogenic for hematologic disorder by Institute of Human Genetics, Heidelberg University

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006363.6(SEC23B):c.1571C>T (p.Ala524Val)	rs398124225	0.00001
NM_001972.4(ELANE):c.641G>A (p.Gly214Glu)	rs1555710089
NM_003126.4(SPTA1):c.4519C>T (p.Arg1507Ter)	rs1651716612

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