List of variants reported as uncertain significance for von Willebrand disease type 1; von Willebrand disease type 3

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000552.5(VWF):c.4196G>A (p.Arg1399His)	rs1800382	0.00907
NM_000552.5(VWF):c.5278G>A (p.Val1760Ile)	rs61750604	0.00094
NM_000552.5(VWF):c.5851A>G (p.Thr1951Ala)	rs144072210	0.00054
NM_000552.5(VWF):c.5665-9C>A	rs201789774	0.00041
NM_000552.5(VWF):c.4842T>G (p.Asp1614Glu)	rs1335546904
NM_000552.5(VWF):c.5793G>C (p.Gln1931His)	rs574811308
NM_000552.5(VWF):c.6535T>C (p.Ser2179Pro)	rs2136385329

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