ClinVar Miner

Submissions for variant NM_001256545.2(MEGF10):c.3384T>C (p.Ser1128=)

dbSNP: rs1055806132
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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 RCV002088023 SCV002372474 likely benign MEGF10-related myopathy 2022-08-15 criteria provided, single submitter clinical testing

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