ClinVar Miner

Submissions for variant NM_000033.4(ABCD1):c.198C>T (p.Gly66=)

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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 RCV003511833 SCV004315313 likely benign Adrenoleukodystrophy 2024-01-07 criteria provided, single submitter clinical testing

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