ClinVar Miner

Submissions for variant NM_000527.4(LDLR):c.1358+32C>T (rs6413505)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000467166 SCV000556784 benign Familial hypercholesterolemia 1 2017-07-27 criteria provided, single submitter clinical testing
Laboratory of Genetics and Molecular Cardiology, University of São Paulo RCV000467166 SCV000588576 benign Familial hypercholesterolemia 1 2016-03-01 criteria provided, single submitter research

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