ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.496+21G>T (rs111033278)

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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 RCV000041294 SCV000064985 benign not specified 2011-06-27 criteria provided, single submitter clinical testing c.496+21G>T in intron 5 of USH1C: This variant is not expected to have clinical significance because it is not located in the conserved region of the splicing c onsensus sequence.

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