ClinVar Miner

Submissions for variant NM_014324.6(AMACR):c.1119T>C (p.Ile373=)

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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 RCV003504870 SCV004317158 likely benign Alpha-methylacyl-CoA racemase deficiency 2023-10-13 criteria provided, single submitter clinical testing

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