ClinVar Miner

Submissions for variant NM_004006.2(DMD):c.1718del (p.Ala573fs) (rs1569229528)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Stanford Center for Inherited Cardiovascular Disease,Stanford University RCV000786281 SCV000925039 pathogenic not provided 2011-08-08 no assertion criteria provided provider interpretation

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