ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.3750+7G>A (rs397516305)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000036125 SCV000059777 likely benign not specified 2010-05-06 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000726843 SCV000703586 uncertain significance not provided 2016-12-06 criteria provided, single submitter clinical testing
Invitae RCV000726843 SCV001062802 likely benign not provided 2020-11-23 criteria provided, single submitter clinical testing
Natera, Inc. RCV001271749 SCV001453175 uncertain significance Usher syndrome, type 1B 2020-04-16 no assertion criteria provided clinical testing

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