ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.8109T>C (p.Asp2703=) (rs201689025)

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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 RCV000570336 SCV000667878 likely benign Hereditary cancer-predisposing syndrome 2016-01-22 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Color RCV000570336 SCV000904744 likely benign Hereditary cancer-predisposing syndrome 2017-11-26 criteria provided, single submitter clinical testing
Invitae RCV000628208 SCV000749102 likely benign Ataxia-telangiectasia syndrome 2017-11-14 criteria provided, single submitter clinical testing

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