ClinVar Miner

Submissions for variant NM_153741.1(DPM3):c.-35-78T>G

dbSNP: rs12745576
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000024455 SCV001782735 likely benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Leiden Muscular Dystrophy (DPM3) RCV000024455 SCV000045751 not provided not provided 2012-04-20 no assertion provided curation

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