ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.7138G>A (p.Asp2380Asn)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003067646 SCV003459613 likely benign Nemaline myopathy 2 2022-07-06 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003491221 SCV004236829 uncertain significance not provided 2023-05-03 criteria provided, single submitter clinical testing

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