ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.5325+156A>G

gnomAD frequency: 0.00395  dbSNP: rs143268615
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001552170 SCV001772817 likely benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001552170 SCV005209187 likely benign not provided criteria provided, single submitter not provided

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