ClinVar Miner

Submissions for variant NM_002838.5(PTPRC):c.558C>T (p.Asn186=)

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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 RCV003628425 SCV004505968 likely benign Immunodeficiency 104 2023-10-16 criteria provided, single submitter clinical testing

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