ClinVar Miner

Submissions for variant NM_014324.6(AMACR):c.663G>A (p.Thr221=)

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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 RCV003854014 SCV004696239 likely benign Alpha-methylacyl-CoA racemase deficiency 2024-05-21 criteria provided, single submitter clinical testing

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