ClinVar Miner

Submissions for variant NM_006790.3(MYOT):c.1275A>T (p.Ala425=)

dbSNP: rs140678912
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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 RCV000639980 SCV000761566 likely benign Myofibrillar myopathy 3 2017-10-11 criteria provided, single submitter clinical testing

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