ClinVar Miner

Submissions for variant NM_001256545.2(MEGF10):c.660-10A>G

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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 RCV005176210 SCV005810711 likely benign MEGF10-related myopathy 2024-04-05 criteria provided, single submitter clinical testing

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