ClinVar Miner

Submissions for variant NM_004817.4(TJP2):c.61-6A>T (rs200415824)

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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 RCV000152017 SCV000200587 uncertain significance not specified 2013-08-30 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000152017 SCV000338547 likely benign not specified 2017-07-05 criteria provided, single submitter clinical testing
Invitae RCV000907762 SCV001052487 likely benign not provided 2020-11-23 criteria provided, single submitter clinical testing
GeneDx RCV000907762 SCV001764131 likely benign not provided 2021-03-25 criteria provided, single submitter clinical testing

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