ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.21262G>A (p.Asp7088Asn)

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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 RCV002882157 SCV003241763 likely benign Nemaline myopathy 2 2023-12-24 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003134518 SCV003810291 uncertain significance not provided 2019-08-08 criteria provided, single submitter clinical testing

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