ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.10921+5G>A

gnomAD frequency: 0.00002  dbSNP: rs398123848
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000080434 SCV000112336 uncertain significance not provided 2013-02-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001086288 SCV001009282 likely benign Duchenne muscular dystrophy 2025-02-03 criteria provided, single submitter clinical testing
Natera, Inc. RCV001826724 SCV002077571 likely benign Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2020-09-09 no assertion criteria provided clinical testing

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