ClinVar Miner

Submissions for variant NM_006231.3(POLE):c.2865-4dup (rs369732588)

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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 RCV000563028 SCV000671315 likely benign Hereditary cancer-predisposing syndrome 2017-02-14 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Other strong data supporting benign classification
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000505870 SCV000602016 likely benign not specified 2017-02-21 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759996 SCV000889736 likely benign not provided 2018-03-02 criteria provided, single submitter clinical testing

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