ClinVar Miner

Submissions for variant NM_017617.5(NOTCH1):c.7096C>T (p.Gln2366Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomics And Bioinformatics Analysis Resource, Columbia University RCV003319954 SCV004024132 likely pathogenic Aortic valve disease 1 no assertion criteria provided research

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