ClinVar Miner

Submissions for variant NM_003647.3(DGKE):c.888+12T>C

gnomAD frequency: 0.00009  dbSNP: rs557770879
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002086821 SCV002328652 likely benign not provided 2024-08-20 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507841 SCV002813719 likely benign Immunoglobulin-mediated membranoproliferative glomerulonephritis 2022-05-26 criteria provided, single submitter clinical testing

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