ClinVar Miner

Submissions for variant NM_001171613.2(PREPL):c.486-18CT[6]

dbSNP: rs750292662
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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 RCV000876062 SCV001018572 likely benign Myasthenic syndrome, congenital, 22 2024-01-01 criteria provided, single submitter clinical testing

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