ClinVar Miner

Submissions for variant NM_000789.4(ACE):c.3380+76G>A

gnomAD frequency: 0.03767  dbSNP: rs4358
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 RCV001663251 SCV001873480 benign not provided 2021-06-18 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001663251 SCV005253018 benign not provided criteria provided, single submitter not provided

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