ClinVar Miner

Submissions for variant NM_012293.3(PXDN):c.621G>T (p.Leu207=)

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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 RCV003870035 SCV004674140 likely benign Anterior segment dysgenesis 7 2023-05-16 criteria provided, single submitter clinical testing

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