ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.734+12G>A

dbSNP: rs876661094
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000218317 SCV000279507 likely benign not specified 2017-11-01 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Color Diagnostics, LLC DBA Color Health RCV000771389 SCV000903728 likely benign Hereditary cancer-predisposing syndrome 2017-03-30 criteria provided, single submitter clinical testing
Invitae RCV002057227 SCV002447472 likely benign Peutz-Jeghers syndrome 2023-06-23 criteria provided, single submitter clinical testing

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