ClinVar Miner

Submissions for variant NM_000384.3(APOB):c.5028C>T (p.Gly1676=) (rs201446451)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000775519 SCV000909883 likely benign Familial hypercholesterolemia 2018-10-18 criteria provided, single submitter clinical testing
Invitae RCV000920366 SCV001065728 likely benign not provided 2018-01-24 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000920366 SCV001250291 likely benign not provided 2019-07-01 criteria provided, single submitter clinical testing

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