ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.598-20G>A

gnomAD frequency: 0.00001  dbSNP: rs747563720
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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 RCV000775652 SCV000910039 likely benign Hereditary cancer-predisposing syndrome 2018-09-24 criteria provided, single submitter clinical testing
Invitae RCV002067323 SCV002354337 likely benign Peutz-Jeghers syndrome 2023-06-20 criteria provided, single submitter clinical testing

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