ClinVar Miner

Submissions for variant NM_031310.3(PLVAP):c.1188G>A (p.Pro396=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003100403 SCV003483780 likely benign not provided 2024-07-19 criteria provided, single submitter clinical testing

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