ClinVar Miner

Submissions for variant NM_000033.4(ABCD1):c.1393+18C>G

gnomAD frequency: 0.00164  dbSNP: rs188551185
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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 RCV001520894 SCV001730107 benign Adrenoleukodystrophy 2024-12-31 criteria provided, single submitter clinical testing

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