ClinVar Miner

Submissions for variant NM_001256545.2(MEGF10):c.117-5_117-4insC

gnomAD frequency: 0.00081  dbSNP: rs538399152
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000268694 SCV000452383 uncertain significance MEGF10-related myopathy 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000268694 SCV000651925 benign MEGF10-related myopathy 2024-01-26 criteria provided, single submitter clinical testing
GeneDx RCV001706568 SCV001893422 benign not provided 2018-07-18 criteria provided, single submitter clinical testing

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