ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.2008A>T (p.Thr670Ser)

dbSNP: rs1476533504
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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 RCV001365321 SCV001561587 likely benign Duchenne muscular dystrophy 2023-07-10 criteria provided, single submitter clinical testing
Natera, Inc. RCV001826039 SCV002092200 uncertain significance Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2019-06-11 no assertion criteria provided clinical testing

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