ClinVar Miner

Submissions for variant NM_001256545.2(MEGF10):c.2857-14T>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002624659 SCV003517611 likely benign MEGF10-related myopathy 2023-09-17 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005034802 SCV005672285 uncertain significance MEGF10-related myopathy; Congenital myopathy 10b, mild variant 2024-03-05 criteria provided, single submitter clinical testing

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