ClinVar Miner

Submissions for variant NM_174936.4(PCSK9):c.240G>A (p.Val80=)

dbSNP: rs2100266566
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001553687 SCV001774645 likely benign not specified 2021-07-18 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004008929 SCV004841197 likely benign Hypercholesterolemia, autosomal dominant, 3 2023-12-18 criteria provided, single submitter clinical testing

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