ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.10087-77G>C

gnomAD frequency: 0.00450  dbSNP: rs143341281
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001546880 SCV001766478 likely benign not provided 2018-07-06 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001546880 SCV005209161 likely benign not provided criteria provided, single submitter not provided

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