ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3557-2dup (rs587779271)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074882 SCV000108095 uncertain significance Lynch syndrome 2013-09-05 reviewed by expert panel research Insufficient evidence
Invitae RCV000557327 SCV000624882 likely benign Hereditary nonpolyposis colon cancer 2017-08-01 criteria provided, single submitter clinical testing

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