ClinVar Miner

Submissions for variant NM_002838.5(PTPRC):c.3852G>A (p.Thr1284=)

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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 RCV003627145 SCV004514098 likely benign Immunodeficiency 104 2023-12-26 criteria provided, single submitter clinical testing

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