List of variants in gene VWF reported as not provided for hematologic disorder

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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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.4751A>G (p.Tyr1584Cys)	rs1800386	0.00237
NM_000552.5(VWF):c.3835G>A (p.Val1279Ile)	rs61749376	0.00048
NM_000552.5(VWF):c.4975C>T (p.Arg1659Ter)	rs61750595	0.00006
NM_000552.5(VWF):c.2446C>T (p.Arg816Trp)	rs121964894	0.00004
NM_000552.5(VWF):c.2372C>T (p.Thr791Met)	rs61748477	0.00001
NM_000552.5(VWF):c.4135C>T (p.Arg1379Cys)	rs61750074	0.00001
NM_000552.5(VWF):c.7603C>T (p.Arg2535Ter)	rs61751296	0.00001
NM_000552.5(VWF):c.2435del (p.Pro812fs)	rs62643632
NM_000552.5(VWF):c.3614G>A (p.Arg1205His)	rs121964895
NM_000552.5(VWF):c.3797C>A (p.Pro1266Gln)	rs61749370
NM_000552.5(VWF):c.3797C>T (p.Pro1266Leu)	rs61749370
NM_000552.5(VWF):c.3916C>T (p.Arg1306Trp)	rs61749384
NM_000552.5(VWF):c.3923G>T (p.Arg1308Leu)	rs61749388
NM_000552.5(VWF):c.3946G>A (p.Val1316Met)	rs61749397
NM_000552.5(VWF):c.4022G>A (p.Arg1341Gln)	rs61749403
NM_000552.5(VWF):c.4273A>T (p.Ile1425Phe)	rs61750083
NM_000552.5(VWF):c.4517C>T (p.Ser1506Leu)	rs61750100
NM_000552.5(VWF):c.4789C>T (p.Arg1597Trp)	rs61750117

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