ClinVar Miner

Submissions for variant NM_000033.4(ABCD1):c.1719G>A (p.Glu573=)

dbSNP: rs2148397951
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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 RCV002141329 SCV002462620 likely benign Adrenoleukodystrophy 2023-06-04 criteria provided, single submitter clinical testing

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