ClinVar Miner

Submissions for variant NM_005591.3(MRE11):c.1404T>C (p.Asp468=) (rs368144567)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000166278 SCV000217059 likely benign Hereditary cancer-predisposing syndrome 2014-10-13 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000328552 SCV000374931 uncertain significance Ataxia-telangiectasia-like disorder 1 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000328552 SCV000764153 likely benign Ataxia-telangiectasia-like disorder 1 2017-12-05 criteria provided, single submitter clinical testing

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