ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.9974+175T>A

dbSNP: rs1602451773
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Undiagnosed Diseases Network, NIH RCV000791277 SCV000930567 pathogenic Duchenne muscular dystrophy 2019-03-05 criteria provided, single submitter clinical testing

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