ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.*24_*28del (rs587779200)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662802 SCV000785622 uncertain significance Hereditary nonpolyposis colorectal cancer type 5 2017-10-16 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759839 SCV000889449 uncertain significance not provided 2017-10-03 criteria provided, single submitter clinical testing
Color RCV001180293 SCV001345187 likely benign Hereditary cancer-predisposing syndrome 2016-10-27 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000074612 SCV000204325 not provided Lynch syndrome 2011-09-21 no assertion provided clinical testing Outside test coverage region (UNCLASSIFED): The *20_*24del variant has not been reported or previously identified by our laboratory. This variant is located in the 3' UTR and its effect on gene expression cannot be determine at this time. Therefore, this variant is of unknown clinical significance.

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