ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.2013T>A (p.Asn671Lys) (rs587779127)

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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) RCV000076360 SCV000107386 uncertain significance Lynch syndrome 2013-09-05 reviewed by expert panel research Insufficient evidence
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759107 SCV000888213 likely pathogenic not provided 2018-01-10 criteria provided, single submitter clinical testing

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