ClinVar Miner

Submissions for variant NM_002838.5(PTPRC):c.299-20A>G

dbSNP: rs377615975
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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 RCV003627061 SCV004386529 likely benign Immunodeficiency 104 2024-01-25 criteria provided, single submitter clinical testing

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