C1264039[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 100453	NM_000552.5(VWF):c.6938G>A (p.Arg2313His)	VWF (R2313H)	Single nucleotide variant (missense variant)	von Willebrand disease type 1 +1 more	GUncertain significance
Select item 619971	NM_000552.5(VWF):c.5851A>G (p.Thr1951Ala)	VWF (T1951A)	Single nucleotide variant (missense variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 801309	NM_000552.5(VWF):c.5665-9C>A	VWF	Single nucleotide variant (intron variant)	not provided +2 more	GUncertain significance
Select item 1033094	NM_000552.5(VWF):c.4492G>A (p.Asp1498Asn)	VWF (D1498N)	Single nucleotide variant (missense variant)	von Willebrand disease type 1	GUncertain significance
Select item 1033091	NM_000552.5(VWF):c.2878C>T (p.Arg960Trp)	VWF (R960W)	Single nucleotide variant (missense variant)	von Willebrand disease type 1	GUncertain significance
Select item 100208	NM_000552.5(VWF):c.2278C>T (p.Arg760Cys)	VWF (R760C)	Single nucleotide variant (missense variant)	von Willebrand disease type 1 +2 more	GConflicting classifications of pathogenicity
Select item 381621	NM_000552.5(VWF):c.1625C>G (p.Ala542Gly)	VWF (A542G)	Single nucleotide variant (missense variant)	VWF-related condition +6 more	GConflicting classifications of pathogenicity
Select item 619940	NM_000552.5(VWF):c.604C>T (p.Arg202Trp)	VWF (R202W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance

ClinVar