ClinVar Miner

Submissions for variant NM_005591.3(MRE11):c.2071-53G>T (rs13447742)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000411487 SCV000488672 benign Ataxia-telangiectasia-like disorder 1 2016-06-09 criteria provided, single submitter clinical testing
GeneDx RCV001546456 SCV001765977 likely benign not provided 2018-12-26 criteria provided, single submitter clinical testing
University of Washington Department of Laboratory Medicine, University of Washington RCV000209483 SCV000265279 likely benign Hereditary cancer-predisposing syndrome 2015-12-01 no assertion criteria provided clinical testing

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