ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.4158C>T (p.Leu1386=)

dbSNP: rs780038701
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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 RCV001433877 SCV001636674 likely benign Duchenne muscular dystrophy 2021-01-31 criteria provided, single submitter clinical testing

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