ClinVar Miner

Submissions for variant NM_001164508.2(NEB):c.8682C>T (p.Ser2894=)

dbSNP: rs373799650
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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 RCV000946145 SCV001092246 likely benign Nemaline myopathy 2 2024-01-17 criteria provided, single submitter clinical testing

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