ClinVar Miner

Submissions for variant NM_001256545.2(MEGF10):c.90C>T (p.Asp30=)

dbSNP: rs140458094
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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 RCV001430521 SCV001633263 likely benign MEGF10-related myopathy 2024-02-06 criteria provided, single submitter clinical testing

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