ClinVar Miner

Submissions for variant NM_003647.3(DGKE):c.798T>A (p.Leu266=)

gnomAD frequency: 0.00312  dbSNP: rs61751970
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001595398 SCV001828760 benign not provided 2021-05-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001595398 SCV002410543 benign not provided 2024-01-26 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002294474 SCV002587722 benign Kidney disorder 2022-04-21 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506700 SCV002798819 likely benign Immunoglobulin-mediated membranoproliferative glomerulonephritis 2021-07-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001595398 SCV005250557 benign not provided criteria provided, single submitter not provided

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