List of variants reported as likely pathogenic for von Willebrand disease type 3 by NIHR Bioresource Rare Diseases, University of Cambridge

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000552.5(VWF):c.2443-1G>C	rs61748480
NM_000552.5(VWF):c.2516del (p.Gly839fs)	rs61748481
NM_000552.5(VWF):c.3675-1G>A	rs746457842
NM_000552.5(VWF):c.533-48_657+52del	rs1591914708
NM_000552.5(VWF):c.7399C>T (p.Gln2467Ter)	rs1591838792
NM_000552.5(VWF):c.7664_7665insAG (p.Cys2557fs)	rs267607364
NM_000552.5(VWF):c.7730-1G>T	rs267607366
NM_000552.5(VWF):c.7863del (p.Thr2622fs)	rs1591834850

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