ClinVar Miner

List of variants in gene VWF reported as pathogenic for Reduced von Willebrand factor activity; Reduced quantity of Von Willebrand factor

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000552.5(VWF):c.658-3C>A	rs377196768	0.00007
NM_000552.5(VWF):c.3614G>A (p.Arg1205His)	rs121964895

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