ClinVar Miner

Submissions for variant NM_006790.3(MYOT):c.156T>C (p.Phe52=)

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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 RCV003018469 SCV003310160 likely benign Myofibrillar myopathy 3 2022-03-04 criteria provided, single submitter clinical testing

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