ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.3277-30C>T

gnomAD frequency: 0.00559  dbSNP: rs72468660
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 RCV001714159 SCV001941335 benign not provided 2018-07-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001714159 SCV005276024 benign not provided criteria provided, single submitter not provided

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