ClinVar Miner

Submissions for variant NM_003647.3(DGKE):c.465-3C>T

gnomAD frequency: 0.00161  dbSNP: rs375726408
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000891624 SCV001035449 likely benign not provided 2025-01-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000891624 SCV005211092 likely benign not provided criteria provided, single submitter not provided
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000891624 SCV001954807 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000891624 SCV001974701 uncertain significance not provided no assertion criteria provided clinical testing

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