ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.20592T>C (p.Ala6864=)

dbSNP: rs754233089
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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 RCV001496866 SCV001701580 likely benign Nemaline myopathy 2 2019-06-19 criteria provided, single submitter clinical testing

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