ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.6095+15T>C (rs3212321)

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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 RCV000128886 SCV000172743 benign Hereditary cancer-predisposing syndrome 2012-08-06 criteria provided, single submitter clinical testing
Color RCV000128886 SCV000682301 benign Hereditary cancer-predisposing syndrome 2015-04-09 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000322367 SCV000367062 likely benign Ataxia-telangiectasia syndrome 2016-06-14 criteria provided, single submitter clinical testing
PreventionGenetics RCV000679132 SCV000805593 benign not specified 2016-10-21 criteria provided, single submitter clinical testing

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