ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.1410-54C>T (rs7633154)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000075196 SCV000106191 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
PreventionGenetics,PreventionGenetics RCV000247033 SCV000303144 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000247033 SCV001156744 benign not specified 2018-07-05 criteria provided, single submitter clinical testing
Color RCV001190168 SCV001357594 benign Hereditary cancer-predisposing syndrome 2018-12-20 criteria provided, single submitter clinical testing

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