ClinVar Miner

Submissions for variant NM_174936.4(PCSK9):c.1212G>C (p.Pro404=)

dbSNP: rs777470856
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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 RCV001194050 SCV001363297 likely benign not specified 2020-01-31 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001525413 SCV001735505 likely benign Familial hypercholesterolemia 2021-01-11 criteria provided, single submitter clinical testing

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