ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.4002-12_4002-10dup

dbSNP: rs59056100
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074979 SCV000108194 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
Mendelics RCV000986751 SCV001135866 benign Lynch syndrome 5 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001618243 SCV001845720 benign not provided 2019-08-13 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002267834 SCV002552380 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001618243 SCV004222032 benign not provided 2023-05-16 criteria provided, single submitter clinical testing

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