ClinVar Miner

Submissions for variant NM_198576.4(AGRN):c.1384+7G>A

dbSNP: rs552044488
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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 RCV001466231 SCV001670231 likely benign Congenital myasthenic syndrome 8 2022-11-28 criteria provided, single submitter clinical testing

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