ClinVar Miner

Submissions for variant NM_138638.5(CFL2):c.94A>C (p.Arg32=)

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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 RCV005180199 SCV005807109 likely benign Nemaline myopathy 7 2024-04-30 criteria provided, single submitter clinical testing

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