ClinVar Miner

Submissions for variant NM_002294.3(LAMP2):c.928+11C>T

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002625596 SCV002955086 likely benign Danon disease 2023-09-26 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003331379 SCV004038089 likely benign not specified 2023-08-19 criteria provided, single submitter clinical testing

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