List of variants reported as likely pathogenic for leukopenia by Genomics England Pilot Project, Genomics England

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_152564.5(VPS13B):c.4949+2T>C	rs761273297	0.00001
NM_152564.5(VPS13B):c.6046+1G>C	rs750003804

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