ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.1167C>T (p.Pro389=) (rs1042819)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000445727 SCV000662363 likely benign Hereditary cancer-predisposing syndrome 2015-01-15 criteria provided, single submitter clinical testing
Color RCV000445727 SCV000537465 likely benign Hereditary cancer-predisposing syndrome 2015-10-19 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000234680 SCV000430959 uncertain significance Lynch syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000524103 SCV000283704 likely benign Hereditary nonpolyposis colon cancer 2017-12-26 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759841 SCV000889454 likely benign not provided 2018-02-13 criteria provided, single submitter clinical testing

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