ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.18871G>A (p.Ala6291Thr)

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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 RCV002624879 SCV003518263 likely benign Nemaline myopathy 2 2023-12-25 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003140138 SCV003814107 uncertain significance not provided 2020-03-20 criteria provided, single submitter clinical testing

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