ClinVar Miner

Submissions for variant NM_001128840.3(CACNA1D):c.1220+678_1220+679insGGG (rs398122827)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000032914 SCV000056686 pathogenic Sinoatrial node dysfunction and deafness 2011-01-01 no assertion criteria provided literature only
University of Washington Center for Mendelian Genomics, University of Washington RCV000032914 SCV001480018 likely pathogenic Sinoatrial node dysfunction and deafness no assertion criteria provided research

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