ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.862+9C>T

dbSNP: rs2080783149
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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 RCV001178214 SCV001342594 uncertain significance Hereditary cancer-predisposing syndrome 2018-12-11 criteria provided, single submitter clinical testing
Invitae RCV003617898 SCV004449132 likely benign Peutz-Jeghers syndrome 2023-03-31 criteria provided, single submitter clinical testing

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