ClinVar Miner

Submissions for variant NM_198576.4(AGRN):c.4106-18C>T

dbSNP: rs919606136
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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 RCV002099066 SCV002440018 likely benign Congenital myasthenic syndrome 8 2021-07-07 criteria provided, single submitter clinical testing

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