ClinVar Miner

Submissions for variant NM_000384.3(APOB):c.9445G>A (p.Asp3149Asn) (rs759354804)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000775474 SCV000909837 likely benign Familial hypercholesterolemia 2017-12-08 criteria provided, single submitter clinical testing
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease,Montreal Heart Institute RCV000845553 SCV000987675 uncertain significance not provided criteria provided, single submitter clinical testing

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