ClinVar Miner

Submissions for variant NC_000001.10:g.(?_216260061)_(216270555_?)del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000156001 SCV000205713 pathogenic Rare genetic deafness 2013-08-01 criteria provided, single submitter clinical testing The Deletion of Exons 22-24 in USH2A has not been reported in the literature nor previously identified by our laboratory. This variant is a multi-exonic deletio n encompassing exons 22-24 of USH2A and is predicted to result in an absent or t runcated protein. Several large deletions that span one or more exons of the USH 2A gene have been reported in probands affected with Usher syndrome type II (Ber nal 2005, Baux 2007, Dreyer 2008, Stabej 2012). In summary, this variant meets o ur criteria to be classified as pathogenic (http:/pcpgm.partners.org/LMM).

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