ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.921-9C>T (rs761688641)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000198987 SCV000253268 likely benign Peutz-Jeghers syndrome 2017-12-11 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000507064 SCV000602243 uncertain significance not specified 2017-02-17 criteria provided, single submitter clinical testing
Color RCV000580751 SCV000686706 likely benign Hereditary cancer-predisposing syndrome 2017-06-05 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000679329 SCV000806095 likely benign not provided 2017-06-20 criteria provided, single submitter clinical testing

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