ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.3603+3dup

dbSNP: rs5902031
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Total submissions: 7
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000176657 SCV000228348 likely benign not specified 2015-04-28 criteria provided, single submitter clinical testing
Invitae RCV001510186 SCV001717157 benign Duchenne muscular dystrophy 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001573481 SCV001941518 benign not provided 2018-06-07 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000176657 SCV001740184 benign not specified no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001573481 SCV001799425 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000176657 SCV001916997 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000176657 SCV001930673 benign not specified no assertion criteria provided clinical testing

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