ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.10910C>T (p.Ser3637Leu)

gnomAD frequency: 0.00001  dbSNP: rs200166885
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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 RCV001048444 SCV001212451 likely benign Duchenne muscular dystrophy 2023-08-22 criteria provided, single submitter clinical testing
Natera, Inc. RCV001832453 SCV002077573 uncertain significance Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2019-07-25 no assertion criteria provided clinical testing

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