List of variants in gene VWF studied for von Willebrand disease type 2N

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000552.5(VWF):c.2561G>A (p.Arg854Gln)	rs41276738	0.00377
NM_000552.5(VWF):c.2635G>A (p.Asp879Asn)	rs61748485	0.00005
NM_000552.5(VWF):c.2446C>T (p.Arg816Trp)	rs121964894	0.00004
NM_000552.5(VWF):c.2435C>T (p.Pro812Leu)	rs62643631	0.00003
NM_000552.5(VWF):c.2372C>T (p.Thr791Met)	rs61748477	0.00001
NM_000552.5(VWF):c.1071C>A (p.Tyr357Ter)	rs61754002
NM_000552.5(VWF):c.2384A>G (p.Tyr795Cys)	rs61748478
NM_000552.5(VWF):c.2411G>T (p.Cys804Phe)	rs62643630
NM_000552.5(VWF):c.2637C>A (p.Asp879Glu)
NM_000552.5(VWF):c.3178T>C (p.Cys1060Arg)	rs61748497

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