List of variants in gene VWF reported as benign by Eurofins NTD LLC (GA)

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.2880G>A (p.Arg960=)	rs1800380	0.25897
NM_000552.5(VWF):c.954T>A (p.Asn318Lys)	rs1800387	0.15296
NM_000552.5(VWF):c.2220G>A (p.Met740Ile)	rs2228317	0.05696
NM_000552.5(VWF):c.5313G>T (p.Gly1771=)	rs2229448	0.00914
NM_000552.5(VWF):c.1329C>T (p.Ser443=)	rs142404899	0.00058

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