ClinVar Miner

Submissions for variant NM_174936.4(PCSK9):c.1355-16C>G

gnomAD frequency: 0.00012  dbSNP: rs28385713
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002162313 SCV002333318 benign Hypercholesterolemia, autosomal dominant, 3 2025-02-02 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003331279 SCV004038370 benign not specified 2023-08-07 criteria provided, single submitter clinical testing

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