ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.375-13C>T

dbSNP: rs1568705244
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000709573 SCV000839412 uncertain significance Peutz-Jeghers syndrome 2018-07-02 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000709573 SCV004829709 likely benign Peutz-Jeghers syndrome 2023-08-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000709573 SCV005818780 likely benign Peutz-Jeghers syndrome 2024-05-01 criteria provided, single submitter clinical testing

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