ClinVar Miner

Submissions for variant NM_022114.4(PRDM16):c.677-16_677-11dup

dbSNP: rs138423019
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001665360 SCV001872722 likely benign not provided 2021-02-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073057 SCV002405951 benign Left ventricular noncompaction 8 2025-01-28 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001700798 SCV005423101 benign not specified 2024-10-06 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001665360 SCV005875842 benign not provided 2024-09-16 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001700798 SCV001924679 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001700798 SCV001952161 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001700798 SCV001965579 benign not specified no assertion criteria provided clinical testing

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