ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.7580T>A (p.Leu2527Ter)

dbSNP: rs1603452200
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV000850325 SCV000992500 pathogenic Myopathy no assertion criteria provided clinical testing

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