ClinVar Miner

Submissions for variant NM_000384.3(APOB):c.4663A>G (p.Ile1555Val) (rs141225768)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Genetics and Molecular Cardiology, University of São Paulo RCV000497186 SCV000588436 uncertain significance Familial hypercholesterolemia 1 2016-03-01 criteria provided, single submitter research
Robarts Research Institute,Western University RCV000497186 SCV000782857 uncertain significance Familial hypercholesterolemia 1 2018-01-02 criteria provided, single submitter clinical testing
Color RCV000771608 SCV000904212 likely benign Familial hypercholesterolemia 2018-03-23 criteria provided, single submitter clinical testing
Invitae RCV000866684 SCV001007814 likely benign not provided 2019-01-02 criteria provided, single submitter clinical testing

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