ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.736-15_736-4dup (rs111033503)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000036249 SCV000059901 benign not specified 2015-07-30 criteria provided, single submitter clinical testing c.736-15_736-4dup in intron 7 of MYO7A: This variant is not expected to have cli nical significance because it has been identified in 6.9% (343/4990) of African chromosomes by the Exome Aggregation Consortium (ExAC, http://exac.broadinstitut; dbSNP rs111537161).
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000224378 SCV000281158 benign not provided 2015-08-26 criteria provided, single submitter clinical testing

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