ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.2922-8T>A (rs545892367)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000727114 SCV000705844 uncertain significance not provided 2017-02-06 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000502033 SCV000593479 likely benign not specified 2016-08-24 criteria provided, single submitter clinical testing
Invitae RCV000547295 SCV000622378 likely benign Ataxia-telangiectasia syndrome 2017-05-01 criteria provided, single submitter clinical testing

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