ClinVar Miner

Submissions for variant NM_022114.4(PRDM16):c.2058G>A (p.Thr686=)

gnomAD frequency: 0.00001  dbSNP: rs368426649
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
GeneDx RCV000651677 SCV000727290 likely benign not provided 2021-05-12 criteria provided, single submitter clinical testing
Invitae RCV001522232 SCV001731729 benign Left ventricular noncompaction 8 2021-07-31 criteria provided, single submitter clinical testing

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