ClinVar Miner

Submissions for variant NM_000033.4(ABCD1):c.906G>A (p.Glu302=)

gnomAD frequency: 0.00001  dbSNP: rs782178199
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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 RCV002087456 SCV002330347 likely benign Adrenoleukodystrophy 2021-08-09 criteria provided, single submitter clinical testing

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