"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "VWA1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2683688	NM_022834.5(VWA1):c.205G>A (p.Gly69Arg)	VWA1 (G69R)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 3379764	NM_022834.5(VWA1):c.586G>A (p.Asp196Asn)	VWA1 (D196N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3379789	NM_022834.5(VWA1):c.1220T>C (p.Phe407Ser)	VWA1 (F407S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

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