ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.291-17del

dbSNP: rs764973846
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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 RCV000581955 SCV000691495 likely benign Hereditary cancer-predisposing syndrome 2017-02-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002061948 SCV002360815 likely benign Peutz-Jeghers syndrome 2024-11-11 criteria provided, single submitter clinical testing

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