ClinVar Miner

Submissions for variant NM_000301.5(PLG):c.1878-17G>A

gnomAD frequency: 0.68619  dbSNP: rs2859879
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001674878 SCV001890740 benign not provided 2021-06-19 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001789504 SCV002031473 benign Angioedema, hereditary, 4 2021-10-25 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001789503 SCV002031474 benign Plasminogen deficiency, type I 2021-10-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001674878 SCV002392844 benign not provided 2024-01-31 criteria provided, single submitter clinical testing

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