ClinVar Miner

Submissions for variant NM_000384.2(APOB):c.12088-13delT (rs751121092)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000582263 SCV000687196 benign Familial hypercholesterolemia 2017-08-28 criteria provided, single submitter clinical testing
Color RCV000776049 SCV000910658 uncertain significance Familial hypercholesterolemias 2018-05-24 criteria provided, single submitter clinical testing

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