ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.10815A>C (p.Lys3605Asn)

gnomAD frequency: 0.00003  dbSNP: rs764516612
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001350621 SCV001545030 likely benign Duchenne muscular dystrophy 2024-10-08 criteria provided, single submitter clinical testing
Natera, Inc. RCV001825965 SCV002077583 uncertain significance Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2019-07-15 no assertion criteria provided clinical testing

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