ClinVar Miner

Submissions for variant NM_001909.5(CTSD):c.228+20C>A

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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 RCV005123803 SCV005741654 likely benign Neuronal ceroid lipofuscinosis 2024-02-26 criteria provided, single submitter clinical testing

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