ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.576C>T (p.Ile192=)

gnomAD frequency: 0.00001  dbSNP: rs878853991
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000773880 SCV000907580 likely benign Hereditary cancer-predisposing syndrome 2018-09-05 criteria provided, single submitter clinical testing
Invitae RCV001441084 SCV001644003 likely benign Peutz-Jeghers syndrome 2023-04-15 criteria provided, single submitter clinical testing
GeneDx RCV001585700 SCV001814041 likely benign not provided 2019-01-18 criteria provided, single submitter clinical testing

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