ClinVar Miner

Submissions for variant NM_000310.4(PPT1):c.234+7C>A

dbSNP: rs200777536
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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 RCV001453600 SCV001657296 likely benign Neuronal ceroid lipofuscinosis 1 2024-01-07 criteria provided, single submitter clinical testing

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