ClinVar Miner

Submissions for variant NM_001909.5(CTSD):c.672G>A (p.Val224=)

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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 RCV003867327 SCV004672462 likely benign Neuronal ceroid lipofuscinosis 2023-12-13 criteria provided, single submitter clinical testing

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