ClinVar Miner

Submissions for variant NM_022114.4(PRDM16):c.2169G>A (p.Ser723=)

gnomAD frequency: 0.00001  dbSNP: rs775363690
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 RCV001913934 SCV002188914 likely benign Left ventricular noncompaction 8 2024-07-19 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001913934 SCV003809838 uncertain significance Left ventricular noncompaction 8 2021-07-07 criteria provided, single submitter clinical testing

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