ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.9564-6T>C

dbSNP: rs876657453
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000213699 SCV000270134 likely benign not specified 2015-06-24 criteria provided, single submitter clinical testing c.9564-6 T>C in exon 66 of DMD: This variant is not expected to have clinical si gnificance because a T>C change at this position does not diverge from the splic e consensus sequence and is therefore unlikely to impact splicing.
Invitae RCV002057102 SCV002418732 likely benign Duchenne muscular dystrophy 2023-07-06 criteria provided, single submitter clinical testing

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