ClinVar Miner

Submissions for variant NM_000033.4(ABCD1):c.658C>T (p.Leu220=)

dbSNP: rs2148389558
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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 RCV002200524 SCV002483592 likely benign Adrenoleukodystrophy 2020-12-19 criteria provided, single submitter clinical testing

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