ClinVar Miner

Submissions for variant NM_198576.4(AGRN):c.2536+14C>T

dbSNP: rs1293258104
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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 RCV002121761 SCV002444676 likely benign Congenital myasthenic syndrome 8 2021-12-02 criteria provided, single submitter clinical testing

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