ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.3433-5_3434del

dbSNP: rs863224994
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000201188 SCV000255722 pathogenic Duchenne muscular dystrophy 2014-07-03 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV001781597 SCV002021041 pathogenic not provided 2020-01-27 criteria provided, single submitter clinical testing

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