ClinVar Miner

Submissions for variant NM_174936.4(PCSK9):c.1503+20GT[17]

dbSNP: rs35115360
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000582680 SCV000690966 likely benign Hypercholesterolemia, familial, 1 2017-08-05 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000775288 SCV000909547 benign Familial hypercholesterolemia 2017-12-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061899 SCV002408475 benign Hypercholesterolemia, autosomal dominant, 3 2025-02-02 criteria provided, single submitter clinical testing

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