ClinVar Miner

Submissions for variant NM_001171613.2(PREPL):c.465T>C (p.Phe155=)

dbSNP: rs2466276978
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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 RCV002613305 SCV002954721 likely benign Myasthenic syndrome, congenital, 22 2022-07-27 criteria provided, single submitter clinical testing

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