List of variants in gene VWF reported by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000552.5(VWF):c.4457C>T (p.Ser1486Leu)	rs149424724	0.00282
NM_000552.5(VWF):c.4751A>G (p.Tyr1584Cys)	rs1800386	0.00237
NM_000552.5(VWF):c.4115T>G (p.Ile1372Ser)	rs61750070	0.00004
NM_000552.5(VWF):c.3797C>A (p.Pro1266Gln)	rs61749370
NM_000552.5(VWF):c.3925A>G (p.Ile1309Val)	rs61749389
NM_000552.5(VWF):c.3946G>A (p.Val1316Met)	rs61749397
NM_000552.5(VWF):c.4082T>C (p.Leu1361Ser)	rs61749408
NM_000552.5(VWF):c.4120C>T (p.Arg1374Cys)	rs61750071

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