ClinVar Miner

Submissions for variant NM_018941.4(CLN8):c.834G>A (p.Gly278=)

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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 RCV003648523 SCV004451849 likely benign Neuronal ceroid lipofuscinosis 2023-04-08 criteria provided, single submitter clinical testing

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