ClinVar Miner

Submissions for variant NM_006231.3(POLE):c.5013C>A (p.Leu1671=) (rs1260912213)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001082550 SCV000653335 likely benign Colorectal cancer, susceptibility to, 12 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000575123 SCV000674319 likely benign Hereditary cancer-predisposing syndrome 2015-07-20 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000553028 SCV001148881 uncertain significance not provided 2017-02-01 criteria provided, single submitter clinical testing

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