ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.375-8C>T

gnomAD frequency: 0.00002  dbSNP: rs528370544
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000941930 SCV001087836 likely benign Peutz-Jeghers syndrome 2024-01-02 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000941930 SCV004828540 likely benign Peutz-Jeghers syndrome 2024-02-05 criteria provided, single submitter clinical testing

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