ClinVar Miner

Submissions for variant NM_002838.5(PTPRC):c.3399A>G (p.Glu1133=)

dbSNP: rs1571896551
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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 RCV000934345 SCV001080066 likely benign Immunodeficiency 104 2023-09-24 criteria provided, single submitter clinical testing

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