ClinVar Miner

Submissions for variant NM_174936.4(PCSK9):c.803T>G (p.Leu268Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004807691 SCV005431383 uncertain significance Hypercholesterolemia, autosomal dominant, 3 2024-03-05 criteria provided, single submitter clinical testing

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