ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.885-81G>C (rs104894999)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Harris Lab, University of Minnesota RCV000114849 SCV000148744 not provided not provided no assertion provided not provided
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000075918 SCV000106937 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%

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