ClinVar Miner

Submissions for variant NM_006493.4(CLN5):c.6G>T (p.Ala2=)

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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 RCV002796336 SCV003201936 likely benign Neuronal ceroid lipofuscinosis 2022-05-11 criteria provided, single submitter clinical testing

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