ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.862+14C>T

gnomAD frequency: 0.00001  dbSNP: rs562847220
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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 RCV001181035 SCV001346090 likely benign Hereditary cancer-predisposing syndrome 2019-06-04 criteria provided, single submitter clinical testing
Invitae RCV002067916 SCV002360023 likely benign Peutz-Jeghers syndrome 2023-10-25 criteria provided, single submitter clinical testing

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