ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.8715A>G (p.Thr2905=) (rs786202933)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000166007 SCV000216766 likely benign Hereditary cancer-predisposing syndrome 2014-10-02 criteria provided, single submitter clinical testing
Invitae RCV000979737 SCV001127682 likely benign Ataxia-telangiectasia syndrome 2019-12-31 criteria provided, single submitter clinical testing
Color RCV000166007 SCV001354846 likely benign Hereditary cancer-predisposing syndrome 2019-12-20 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV001201196 SCV001372267 likely benign not specified 2020-06-27 criteria provided, single submitter clinical testing

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