ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.863-12G>A

gnomAD frequency: 0.00002  dbSNP: rs753729414
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002109495 SCV002392636 likely benign Peutz-Jeghers syndrome 2023-10-05 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256920 SCV002526950 uncertain significance Hereditary cancer-predisposing syndrome 2022-01-22 criteria provided, single submitter curation
All of Us Research Program, National Institutes of Health RCV002109495 SCV004818141 likely benign Peutz-Jeghers syndrome 2023-03-23 criteria provided, single submitter clinical testing

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