ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.734+17C>A

dbSNP: rs751929304
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000581710 SCV000691538 likely benign Hereditary cancer-predisposing syndrome 2017-04-24 criteria provided, single submitter clinical testing
Counsyl RCV000662414 SCV000784848 likely benign Peutz-Jeghers syndrome 2017-01-19 criteria provided, single submitter clinical testing
Invitae RCV000662414 SCV002396114 likely benign Peutz-Jeghers syndrome 2023-12-22 criteria provided, single submitter clinical testing

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