ClinVar Miner

Submissions for variant NM_000033.4(ABCD1):c.173C>T (p.Ser58Phe)

dbSNP: rs781943986
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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 RCV001443055 SCV001646015 likely benign Adrenoleukodystrophy 2024-10-21 criteria provided, single submitter clinical testing

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