ClinVar Miner

Submissions for variant NM_000051.3(ATM):c.2838+9C>G (rs370160823)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000579471 SCV000682081 likely benign Hereditary cancer-predisposing syndrome 2017-05-16 criteria provided, single submitter clinical testing
GeneDx RCV000427251 SCV000517981 benign not specified 2015-09-01 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV000198514 SCV000252950 likely benign Ataxia-telangiectasia syndrome 2016-12-13 criteria provided, single submitter clinical testing

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