ClinVar Miner

Submissions for variant NM_174936.4(PCSK9):c.1503+20GT[14]

dbSNP: rs35115360
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000582311 SCV000690963 likely benign Hypercholesterolemia, familial, 1 2017-10-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002529276 SCV003477530 likely benign Hypercholesterolemia, autosomal dominant, 3 2022-11-12 criteria provided, single submitter clinical testing

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