ClinVar Miner

Variants in gene VWF with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 12
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HGVS dbSNP
NM_000552.4(VWF):c.1110-7dup rs534403271
NM_000552.4(VWF):c.1614C>T (p.Pro538=) rs138268387
NM_000552.4(VWF):c.1728G>T (p.Met576Ile) rs150146744
NM_000552.4(VWF):c.2365A>G (p.Thr789Ala) rs1063856
NM_000552.4(VWF):c.3686T>G (p.Val1229Gly) rs61749367
NM_000552.4(VWF):c.3692A>C (p.Asn1231Thr) rs61749368
NM_000552.4(VWF):c.3719C>T (p.Pro1240Leu) rs150576611
NM_000552.4(VWF):c.4641T>C (p.Thr1547=) rs216310
NM_000552.4(VWF):c.5170+10C>T rs61750601
NM_000552.4(VWF):c.5277C>T (p.Asp1759=) rs41276736
NM_000552.4(VWF):c.5312-19A>C rs200237834
NM_000552.4(VWF):c.546G>A (p.Ser182=) rs143054357

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