ClinVar Miner

Submissions for variant NM_000033.4(ABCD1):c.912C>G (p.Ala304=)

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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 RCV003511786 SCV004317937 likely benign Adrenoleukodystrophy 2024-02-02 criteria provided, single submitter clinical testing

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