ClinVar Miner

Submissions for variant NM_033337.2(CAV3):c.-106G>A

gnomAD frequency: 0.24982  dbSNP: rs2072583
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000024437 SCV001865362 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Leiden Muscular Dystrophy (CAV3) RCV000024437 SCV000045732 not provided not provided 2012-04-15 no assertion provided curation

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