ClinVar Miner

Submissions for variant NM_002838.5(PTPRC):c.659-12del

dbSNP: rs539544931
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001517907 SCV001726507 benign Immunodeficiency 104 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001587452 SCV001822801 likely benign not provided 2018-07-16 criteria provided, single submitter clinical testing

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