ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.2115C>T (p.Tyr705=) (rs876659149)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000218925 SCV000275271 likely benign Hereditary cancer-predisposing syndrome 2015-04-27 criteria provided, single submitter clinical testing
Invitae RCV000988664 SCV000558352 likely benign Ataxia-telangiectasia syndrome 2019-12-31 criteria provided, single submitter clinical testing
Color RCV000218925 SCV000682025 likely benign Hereditary cancer-predisposing syndrome 2017-01-06 criteria provided, single submitter clinical testing
Mendelics RCV000988664 SCV001138467 likely benign Ataxia-telangiectasia syndrome 2019-05-28 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV001174580 SCV001337758 likely benign not specified 2020-01-10 criteria provided, single submitter clinical testing

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