ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3610G>A (p.Ala1204Thr) (rs869312799)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Washington Department of Laboratory Medicine, University of Washington RCV000210134 SCV000266210 uncertain significance Lynch syndrome 2015-11-20 criteria provided, single submitter clinical testing
Counsyl RCV000663332 SCV000786606 uncertain significance Hereditary nonpolyposis colorectal cancer type 5 2018-06-07 criteria provided, single submitter clinical testing
Ambry Genetics RCV001020725 SCV001182238 uncertain significance Hereditary cancer-predisposing syndrome 2018-09-21 criteria provided, single submitter clinical testing Insufficient evidence

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