ClinVar Miner

Submissions for variant NM_174936.4(PCSK9):c.45G>A (p.Leu15=)

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Total submissions: 2
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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 RCV004807675 SCV005431347 likely benign Hypercholesterolemia, autosomal dominant, 3 2024-07-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV004807675 SCV005813400 likely benign Hypercholesterolemia, autosomal dominant, 3 2024-05-04 criteria provided, single submitter clinical testing

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