ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.402T>C (p.Cys134=)

dbSNP: rs778868074
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001439498 SCV001642387 likely benign Peutz-Jeghers syndrome 2024-02-01 criteria provided, single submitter clinical testing

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