ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.1084T>C (p.Leu362=)

dbSNP: rs1556876311
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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 RCV000630608 SCV000751573 likely benign Duchenne muscular dystrophy 2024-09-11 criteria provided, single submitter clinical testing
Natera, Inc. RCV001835885 SCV002090414 likely benign Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2021-02-18 no assertion criteria provided clinical testing

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