ClinVar Miner

Submissions for variant NM_000033.4(ABCD1):c.1683C>T (p.Asp561=)

dbSNP: rs199997983
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001087253 SCV001020154 likely benign Adrenoleukodystrophy 2022-07-12 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000675194 SCV000800836 likely benign not provided 2015-10-22 no assertion criteria provided clinical testing

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