ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.8995-14del

dbSNP: rs770495295
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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 RCV002213145 SCV002362829 benign Nemaline myopathy 2 2024-01-18 criteria provided, single submitter clinical testing

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