ClinVar Miner

Submissions for variant NM_002659.4(PLAUR):c.24G>A (p.Pro8=)

gnomAD frequency: 0.00621  dbSNP: rs62639324
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000950489 SCV001096802 benign not provided 2018-05-21 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000950489 SCV004139680 likely benign not provided 2023-01-01 criteria provided, single submitter clinical testing PLAUR: BP4, BP7, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000950489 SCV005308093 benign not provided criteria provided, single submitter not provided

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