ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.8669-75C>G

gnomAD frequency: 0.06936  dbSNP: rs17338583
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000508094 SCV000603331 benign not specified 2018-09-24 criteria provided, single submitter clinical testing
GeneDx RCV001698510 SCV001916736 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001698510 SCV005275979 benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV001834637 SCV002087655 benign Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2019-07-26 no assertion criteria provided clinical testing

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