ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.4002-11_4002-10dup

dbSNP: rs59056100
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074978 SCV000108193 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002267833 SCV002552379 benign not specified 2023-08-15 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV003477463 SCV004222031 benign not provided 2023-07-27 criteria provided, single submitter clinical testing

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