ClinVar Miner

Submissions for variant NM_002838.5(PTPRC):c.2179+8C>T

dbSNP: rs369017416
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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 RCV002210774 SCV002491701 likely benign Immunodeficiency 104 2021-07-04 criteria provided, single submitter clinical testing

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