ClinVar Miner

Submissions for variant NM_001171613.2(PREPL):c.485+8A>G

dbSNP: rs2103967683
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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 RCV001423248 SCV001625821 likely benign Myasthenic syndrome, congenital, 22 2020-10-16 criteria provided, single submitter clinical testing

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