ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.291-18C>T

gnomAD frequency: 0.00001  dbSNP: rs1176351456
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000600050 SCV000719031 likely benign not specified 2017-05-01 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV002529534 SCV003021797 likely benign Peutz-Jeghers syndrome 2024-01-17 criteria provided, single submitter clinical testing

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