ClinVar Miner

List of variants in gene VWF reported as likely benign by GeneDx

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Gene type:
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Total variants: 11
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HGVS dbSNP gnomAD frequency
NM_000552.5(VWF):c.3686T>G (p.Val1229Gly) rs61749367 0.00656
NM_000552.5(VWF):c.391G>A (p.Gly131Ser) rs76505074 0.00651
NM_000552.5(VWF):c.1728G>T (p.Met576Ile) rs150146744 0.00155
NM_000552.5(VWF):c.3789G>A (p.Ser1263=) rs199831474 0.00146
NM_000552.5(VWF):c.7082-13G>C rs71581025 0.00108
NM_000552.5(VWF):c.3675-14G>A rs1369248196 0.00006
NM_000552.5(VWF):c.6599-5dup rs768221292 0.00001
NM_000552.5(VWF):c.1110-6dup rs534403271
NM_000552.5(VWF):c.3692A>C (p.Asn1231Thr) rs61749368
NM_000552.5(VWF):c.3692A>G (p.Asn1231Ser) rs61749368
NM_000552.5(VWF):c.7730-177G>T rs573460498

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