ClinVar Miner

Submissions for variant NM_002838.5(PTPRC):c.1479C>G (p.Val493=)

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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 RCV003628063 SCV004425004 likely benign Immunodeficiency 104 2022-12-30 criteria provided, single submitter clinical testing

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