List of variants reported as uncertain significance for Hereditary von Willebrand disease by NIHR Bioresource Rare Diseases, University of Cambridge

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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_000552.5(VWF):c.7940C>T (p.Thr2647Met)	rs61751302	0.00352
NM_000552.5(VWF):c.1463C>G (p.Ala488Gly)	rs144817575	0.00098
NM_000552.5(VWF):c.3835G>A (p.Val1279Ile)	rs61749376	0.00048
NM_000552.5(VWF):c.4146G>T (p.Leu1382=)	rs140464171	0.00044
NM_000552.5(VWF):c.4027A>G (p.Ile1343Val)	rs150923481	0.00016
NM_000552.5(VWF):c.7135C>T (p.Arg2379Cys)	rs61751283	0.00006
NM_000552.5(VWF):c.1514G>A (p.Arg505His)	rs139830291	0.00004
NM_000552.5(VWF):c.6611C>T (p.Pro2204Leu)	rs777556669	0.00004
NM_000552.5(VWF):c.6421G>A (p.Val2141Ile)	rs923531708	0.00003
NM_000552.5(VWF):c.8276T>C (p.Met2759Thr)	rs776681874	0.00002
NM_000552.5(VWF):c.1001G>A (p.Gly334Glu)	rs932134873	0.00001
NM_000552.5(VWF):c.2570A>G (p.Asn857Ser)	rs765163545	0.00001
NM_000552.5(VWF):c.3108+5G>A	rs61748495	0.00001
NM_000552.5(VWF):c.3251G>A (p.Cys1084Tyr)	rs759805079	0.00001
NM_000552.5(VWF):c.5668G>A (p.Gly1890Arg)	rs746837624	0.00001
NM_000552.5(VWF):c.182T>C (p.Leu61Pro)	rs1306914162
NM_000552.5(VWF):c.1841C>T (p.Ser614Phe)	rs776987924
NM_000552.5(VWF):c.2299T>C (p.Cys767Arg)	rs1591880825
NM_000552.5(VWF):c.2686-7T>G	rs1591871882
NM_000552.5(VWF):c.2981G>A (p.Gly994Asp)	rs1591867991
NM_000552.5(VWF):c.435C>G (p.Asn145Lys)	rs1591924311
NM_000552.5(VWF):c.4622A>G (p.Gln1541Arg)	rs1591862393
NM_000552.5(VWF):c.4727C>A (p.Thr1576Asn)	rs1591862230
NM_000552.5(VWF):c.4834G>C (p.Ala1612Pro)	rs1591862118
NM_000552.5(VWF):c.5170+5G>A	rs1591860863
NM_000552.5(VWF):c.5849G>A (p.Cys1950Tyr)	rs1591849732
NM_000552.5(VWF):c.6314C>T (p.Thr2105Ile)	rs761604165
NM_000552.5(VWF):c.6538T>C (p.Tyr2180His)	rs1591848338
NM_000552.5(VWF):c.6762C>G (p.Cys2254Trp)	rs1232884671
NM_000552.5(VWF):c.814G>C (p.Ala272Pro)	rs747799959
NM_000552.5(VWF):c.8215T>C (p.Cys2739Arg)	rs1591827147
NM_000552.5(VWF):c.8275A>G (p.Met2759Val)	rs776211115
NM_000552.5(VWF):c.8307C>A (p.Asp2769Glu)	rs1591826730

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