ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.734+12G>C

gnomAD frequency: 0.00001  dbSNP: rs876661094
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003067086 SCV003453192 likely benign Peutz-Jeghers syndrome 2024-11-15 criteria provided, single submitter clinical testing

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