ClinVar Miner

Submissions for variant NM_198576.4(AGRN):c.5981-16A>G

dbSNP: rs2100703621
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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 RCV002167354 SCV002339052 likely benign Congenital myasthenic syndrome 8 2022-01-14 criteria provided, single submitter clinical testing

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