ClinVar Miner

Submissions for variant NM_002838.5(PTPRC):c.2316C>T (p.Gly772=)

gnomAD frequency: 0.16920  dbSNP: rs7540378
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001513694 SCV001721355 benign Immunodeficiency 104 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001615187 SCV001838593 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001615187 SCV005287962 benign not provided criteria provided, single submitter not provided

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