List of variants in gene VWF reported as pathogenic for von Willebrand disease type 2M

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000552.5(VWF):c.3970G>A (p.Gly1324Ser)	rs61749398	0.00001
NM_000552.5(VWF):c.3854C>T (p.Ser1285Phe)	rs61749380
NM_000552.5(VWF):c.4213AAG[3] (p.Lys1408del)	rs61750078

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