ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.863-20C>T

gnomAD frequency: 0.00001  dbSNP: rs1250319696
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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 RCV001191409 SCV001359230 likely benign Hereditary cancer-predisposing syndrome 2018-12-04 criteria provided, single submitter clinical testing
Invitae RCV003617914 SCV004536474 likely benign Peutz-Jeghers syndrome 2023-02-27 criteria provided, single submitter clinical testing

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