ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.3030C>T (p.Asn1010=) (rs876660913)

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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 RCV000213723 SCV000278719 likely benign Hereditary cancer-predisposing syndrome 2015-09-21 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Color RCV000213723 SCV000682098 likely benign Hereditary cancer-predisposing syndrome 2017-03-08 criteria provided, single submitter clinical testing
Invitae RCV000465401 SCV000558424 likely benign Ataxia-telangiectasia syndrome 2017-12-30 criteria provided, single submitter clinical testing

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