ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.591A>T (p.Gly197=) (rs587780630)

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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 RCV000165264 SCV000215980 likely benign Hereditary cancer-predisposing syndrome 2014-07-30 criteria provided, single submitter clinical testing
Color RCV000165264 SCV000682290 likely benign Hereditary cancer-predisposing syndrome 2016-06-20 criteria provided, single submitter clinical testing
Invitae RCV000122862 SCV000166120 likely benign Ataxia-telangiectasia syndrome 2017-11-20 criteria provided, single submitter clinical testing
PreventionGenetics RCV000254428 SCV000301677 likely benign not specified criteria provided, single submitter clinical testing

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