ClinVar Miner

Submissions for variant NM_000384.3(APOB):c.9226C>A (p.Leu3076Met) (rs72653099)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000471629 SCV000554796 likely benign Hypercholesterolemia, autosomal dominant, type B; Hypobetalipoproteinemia, familial, 1 2017-08-17 criteria provided, single submitter clinical testing
Color RCV000775479 SCV000909842 likely benign Familial hypercholesterolemias 2018-04-20 criteria provided, single submitter clinical testing

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