ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.465-19G>A

gnomAD frequency: 0.00001  dbSNP: rs776367814
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001178796 SCV001343315 uncertain significance Hereditary cancer-predisposing syndrome 2019-01-16 criteria provided, single submitter clinical testing
Invitae RCV001875911 SCV002178589 likely benign Peutz-Jeghers syndrome 2024-01-03 criteria provided, single submitter clinical testing

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