ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.458-17A>G (rs554847828)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000774587 SCV000908346 uncertain significance Hereditary cancer-predisposing syndrome 2018-05-17 criteria provided, single submitter clinical testing
Counsyl RCV000662516 SCV000785060 likely benign Hereditary nonpolyposis colorectal cancer type 5 2017-03-28 criteria provided, single submitter clinical testing
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074999 SCV000108217 uncertain significance Lynch syndrome 2013-09-05 reviewed by expert panel research Insufficient evidence

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