C1264040[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2582351	NM_000552.5(VWF):c.7393G>A (p.Val2465Met)	VWF (V2465M)	Single nucleotide variant (missense variant)	von Willebrand disease type 2	GLikely pathogenic
Select item 619971	NM_000552.5(VWF):c.5851A>G (p.Thr1951Ala)	VWF (T1951A)	Single nucleotide variant (missense variant)	Hereditary von Willebrand disease +6 more	GConflicting classifications of pathogenicity
Select item 100337	NM_000552.5(VWF):c.4195C>T (p.Arg1399Cys)	VWF (R1399C)	Single nucleotide variant (missense variant)	von Willebrand disorder +3 more	GConflicting classifications of pathogenicity
Select item 100208	NM_000552.5(VWF):c.2278C>T (p.Arg760Cys)	VWF (R760C)	Single nucleotide variant (missense variant)	not provided +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 disorder +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