ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.291-20C>T

dbSNP: rs973142127
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002132817 SCV002436238 likely benign Peutz-Jeghers syndrome 2021-03-23 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002132817 SCV006089140 likely benign Peutz-Jeghers syndrome 2025-03-25 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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