ClinVar Miner

Submissions for variant NM_000033.4(ABCD1):c.32G>C (p.Arg11Pro)

dbSNP: rs782122122
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001483807 SCV001688214 likely benign Adrenoleukodystrophy 2024-11-18 criteria provided, single submitter clinical testing
New York Genome Center RCV001483807 SCV002548959 uncertain significance Adrenoleukodystrophy 2021-09-17 criteria provided, single submitter clinical testing

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