ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.7983G>T (p.Trp2661Cys)

dbSNP: rs756956766
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001059963 SCV001224619 likely benign Nemaline myopathy 2 2023-11-05 criteria provided, single submitter clinical testing
Natera, Inc. RCV001059963 SCV002079638 uncertain significance Nemaline myopathy 2 2020-12-15 no assertion criteria provided clinical testing

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