List of variants reported as likely pathogenic for leukopenia by NIHR Bioresource Rare Diseases, University of Cambridge

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_032383.5(HPS3):c.1870G>T (p.Glu624Ter)	rs200079039	0.00003
NM_000760.4(CSF3R):c.340C>T (p.Gln114Ter)	rs756667927	0.00001
NM_000760.4(CSF3R):c.1576+1G>A	rs1031224658
NM_006118.4(HAX1):c.182T>G (p.Phe61Cys)	rs146452018

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