ClinVar Miner

Submissions for variant NM_014324.6(AMACR):c.657C>T (p.Phe219=)

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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 RCV003505770 SCV004251359 likely benign Alpha-methylacyl-CoA racemase deficiency 2024-10-08 criteria provided, single submitter clinical testing

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