ClinVar Miner

List of variants in gene VWF reported as likely benign for von Willebrand disease type 3

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.2771G>A (p.Arg924Gln)	rs33978901	0.01237
NM_000552.5(VWF):c.5170+10C>T	rs61750601	0.00400

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