ClinVar Miner

Submissions for variant NM_006231.3(POLE):c.4952+17_4952+19dupCGT (rs571641918)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000409961 SCV000488857 likely benign Colorectal cancer, susceptibility to, 12 2016-07-05 criteria provided, single submitter clinical testing
GeneDx RCV000484948 SCV000567813 benign not specified 2017-05-23 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.
PreventionGenetics,PreventionGenetics RCV000484948 SCV000806793 benign not specified 2017-02-20 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000484948 SCV000806794 benign not specified 2017-08-11 criteria provided, single submitter clinical testing

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