ClinVar Miner

Submissions for variant NM_000789.4(ACE):c.2598C>G (p.Ala866=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005138523 SCV005763331 likely benign not provided 2024-08-30 criteria provided, single submitter clinical testing

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