ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.8571T>C (p.Ala2857=) (rs786203050)

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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 RCV000166185 SCV000216961 likely benign Hereditary cancer-predisposing syndrome 2014-10-17 criteria provided, single submitter clinical testing
Color RCV000166185 SCV000904755 likely benign Hereditary cancer-predisposing syndrome 2018-07-03 criteria provided, single submitter clinical testing
Invitae RCV000528790 SCV000622830 likely benign Ataxia-telangiectasia syndrome 2017-02-15 criteria provided, single submitter clinical testing

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