ClinVar Miner

Submissions for variant NM_018941.4(CLN8):c.324G>T (p.Thr108=)

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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 RCV003648414 SCV004504871 likely benign Neuronal ceroid lipofuscinosis 2023-02-22 criteria provided, single submitter clinical testing

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