ClinVar Miner

Submissions for variant NM_006231.3(POLE):c.4353G>A (p.Leu1451=) (rs769149466)

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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 RCV000572259 SCV000676215 likely benign Hereditary cancer-predisposing syndrome 2015-11-20 criteria provided, single submitter clinical testing
Invitae RCV000231335 SCV000289376 likely benign Colorectal cancer, susceptibility to, 12 2016-11-10 criteria provided, single submitter clinical testing
PreventionGenetics RCV000679635 SCV000806780 likely benign not provided 2017-10-26 criteria provided, single submitter clinical testing

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