ClinVar Miner

Submissions for variant NM_001042432.2(CLN3):c.264A>G (p.Ser88=)

dbSNP: rs751321507
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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 RCV002193478 SCV002486021 likely benign Neuronal ceroid lipofuscinosis 2022-04-13 criteria provided, single submitter clinical testing

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