ClinVar Miner

Submissions for variant NM_000033.4(ABCD1):c.423C>T (p.Ala141=)

dbSNP: rs2091706712
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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 RCV002128334 SCV002454805 likely benign Adrenoleukodystrophy 2020-12-18 criteria provided, single submitter clinical testing

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