List of variants in gene VWF reported as pathogenic by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000552.5(VWF):c.2561G>A (p.Arg854Gln)	rs41276738	0.00377
NM_000552.5(VWF):c.3390C>T (p.Cys1130=)	rs1591865617	0.00001
NM_000552.5(VWF):c.1117C>T (p.Arg373Ter)	rs62643625
NM_000552.5(VWF):c.2067C>A (p.Cys689Ter)
NM_000552.5(VWF):c.4120C>T (p.Arg1374Cys)	rs61750071

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