ClinVar Miner

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

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Total variants: 10
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NM_000552.4(VWF):c.1583A>G (p.Asn528Ser) rs61754010
NM_000552.4(VWF):c.1648G>A (p.Gly550Arg) rs61754011
NM_000552.4(VWF):c.3814T>C (p.Cys1272Arg) rs61749372
NM_000552.4(VWF):c.4541T>G (p.Phe1514Cys) rs61750101
NM_000552.4(VWF):c.4789C>T (p.Arg1597Trp) rs61750117
NM_000552.4(VWF):c.4820T>A (p.Val1607Asp) rs61750579
NM_000552.4(VWF):c.4837T>C (p.Ser1613Pro) rs61750581
NM_000552.4(VWF):c.4883T>C (p.Ile1628Thr) rs61750584
NM_000552.4(VWF):c.8317T>C (p.Cys2773Arg) rs61751310
VWF, 6-BP INS, NT1212

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