List of variants reported as likely pathogenic for Von Willebrand disease type 2B

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000552.5(VWF):c.7987C>T (p.Arg2663Cys)	rs370662678	0.00004
NM_000552.5(VWF):c.3845T>C (p.Leu1282Pro)	rs61749378
NM_000552.5(VWF):c.3929C>T (p.Ser1310Phe)	rs61749390
NM_000552.5(VWF):c.573G>C (p.Trp191Cys)	rs2497272240

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