ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.777C>T (p.Asn259=) (rs786201105)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000162671 SCV000213118 likely benign Hereditary cancer-predisposing syndrome 2013-01-15 criteria provided, single submitter clinical testing
Invitae RCV000205472 SCV000261777 likely benign Peutz-Jeghers syndrome 2017-02-23 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000679323 SCV000806085 likely benign not provided 2017-11-29 criteria provided, single submitter clinical testing

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