ClinVar Miner

Submissions for variant NM_000487.6(ARSA):c.1108-8G>A

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003501996 SCV004311073 likely benign Metachromatic leukodystrophy 2023-10-30 criteria provided, single submitter clinical testing

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