ClinVar Miner

Submissions for variant NM_174936.4(PCSK9):c.1354+1G>A

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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 RCV004807708 SCV005431415 uncertain significance Hypercholesterolemia, autosomal dominant, 3 2024-08-06 criteria provided, single submitter clinical testing

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