ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.1983T>C (p.Ser661=)

dbSNP: rs1603636536
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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 RCV001438524 SCV001641401 likely benign Duchenne muscular dystrophy 2024-10-05 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832201 SCV002092204 likely benign Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2021-05-15 no assertion criteria provided clinical testing

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