ClinVar Miner

Submissions for variant NM_000527.5(LDLR):c.673_681dup (p.Lys225_Asp227dup)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
LDLR-LOVD, British Heart Foundation RCV000238131 SCV000294887 likely pathogenic Hypercholesterolemia, familial, 1 2016-03-25 criteria provided, single submitter literature only
Centre de Génétique Moléculaire et Chromosomique, Unité de génétique de l'Obésité et des Dyslipidémies, APHP, GH Hôpitaux Universitaires Pitié-Salpêtrière / Charles-Foix RCV000238131 SCV000503214 likely pathogenic Hypercholesterolemia, familial, 1 2016-12-16 criteria provided, single submitter clinical testing subject mutated among 2600 FH index cases screened = 2 , family member = 1
Laboratory of Genetics and Molecular Cardiology, University of São Paulo RCV000238131 SCV000588510 likely pathogenic Hypercholesterolemia, familial, 1 2016-03-01 criteria provided, single submitter research
Laboratory of molecular diagnosis of dyslipidemias, Università egli studi di Napoli Federico II RCV000238131 SCV001653602 likely pathogenic Hypercholesterolemia, familial, 1 2021-05-24 criteria provided, single submitter clinical testing

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