ClinVar Miner

Submissions for variant NM_005591.3(MRE11):c.942A>G (p.Leu314=) (rs1555012700)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000561774 SCV000669643 likely benign Hereditary cancer-predisposing syndrome 2016-02-11 criteria provided, single submitter clinical testing
Invitae RCV000642469 SCV000764151 likely benign Ataxia-telangiectasia-like disorder 1 2017-11-09 criteria provided, single submitter clinical testing

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