ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.1413+13C>T (rs876657623)

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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, Partners HealthCare Personalized Medicine RCV000215236 SCV000271145 likely benign not specified 2015-02-04 criteria provided, single submitter clinical testing c.1413+13C>T in intron 16 of USH1C: This variant is not expected to have clinica l significance because it does not alter an amino acid residue and is not locate d within the splice consensus sequence.

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