ClinVar Miner

Submissions for variant NC_000013.11:g.(?_90698351)_(90699137_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostics Lab, Nemours Children's Health, Delaware RCV000498711 SCV000590841 pathogenic Feingold syndrome type 2 2015-04-27 criteria provided, single submitter clinical testing

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