ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.828A>G (p.Gln276=)

dbSNP: rs2063889616
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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 RCV001038523 SCV001201996 likely benign Duchenne muscular dystrophy 2024-08-28 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832388 SCV002090468 uncertain significance Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2021-09-02 no assertion criteria provided clinical testing

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