ClinVar Miner

Submissions for variant NM_174936.4(PCSK9):c.1378del (p.Val460fs)

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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 RCV004017073 SCV004842415 likely benign Hypercholesterolemia, autosomal dominant, 3 2024-02-05 criteria provided, single submitter clinical testing

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