ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.7281A>T (p.Leu2427=)

dbSNP: rs886038872
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000536258 SCV000625956 likely benign Duchenne muscular dystrophy 2023-10-03 criteria provided, single submitter clinical testing
Natera, Inc. RCV001829556 SCV002087781 likely benign Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2019-07-16 no assertion criteria provided clinical testing

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