ClinVar Miner

Submissions for variant NM_001042432.2(CLN3):c.651G>C (p.Leu217=)

dbSNP: rs2141712068
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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 RCV001427286 SCV001629961 likely benign Neuronal ceroid lipofuscinosis 2020-08-14 criteria provided, single submitter clinical testing

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