ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.465-8G>A

gnomAD frequency: 0.00001  dbSNP: rs878853990
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000231331 SCV000284868 likely benign Peutz-Jeghers syndrome 2023-05-24 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000508005 SCV000602227 uncertain significance not specified 2017-03-02 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001183560 SCV001349341 likely benign Hereditary cancer-predisposing syndrome 2024-01-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000231331 SCV002057251 uncertain significance Peutz-Jeghers syndrome 2021-07-15 criteria provided, single submitter clinical testing

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