ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.290+13T>G

dbSNP: rs1568690565
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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 RCV000772399 SCV000905577 likely benign Hereditary cancer-predisposing syndrome 2018-03-27 criteria provided, single submitter clinical testing
Invitae RCV002534019 SCV003450583 likely benign Peutz-Jeghers syndrome 2022-02-04 criteria provided, single submitter clinical testing

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