ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.2622+33A>G

gnomAD frequency: 0.00546  dbSNP: rs72468678
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000080515 SCV000112417 benign not specified 2017-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001610368 SCV001832971 benign not provided 2018-07-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001610368 SCV005276035 benign not provided criteria provided, single submitter not provided

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