ClinVar Miner

Submissions for variant NM_000439.5(PCSK1):c.239G>A (p.Arg80Gln)

dbSNP: rs1799904
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001822203 SCV002069779 likely benign not specified 2017-07-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002077275 SCV002394016 benign not provided 2023-04-09 criteria provided, single submitter clinical testing

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