ClinVar Miner

Submissions for variant NM_031310.3(PLVAP):c.714T>G (p.Arg238=)

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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 RCV003040179 SCV003348017 likely benign not provided 2022-04-28 criteria provided, single submitter clinical testing

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