ClinVar Miner

Submissions for variant NM_001281492.1(MSH6):c.3611+10dup (rs730882138)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000161948 SCV000211933 likely benign Hereditary nonpolyposis colon cancer 2017-11-24 criteria provided, single submitter clinical testing
Counsyl RCV000409136 SCV000489649 likely benign Hereditary nonpolyposis colorectal cancer type 5 2016-10-31 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000500345 SCV000595845 likely benign not specified 2017-04-12 criteria provided, single submitter clinical testing
Color RCV000580604 SCV000685475 likely benign Hereditary cancer-predisposing syndrome 2015-02-23 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759149 SCV000888286 likely benign not provided 2017-07-26 criteria provided, single submitter clinical testing

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