ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.354C>T (p.Tyr118=)

dbSNP: rs1555737439
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000582051 SCV000691498 likely benign Hereditary cancer-predisposing syndrome 2016-03-23 criteria provided, single submitter clinical testing
Invitae RCV002529284 SCV002944290 likely benign Peutz-Jeghers syndrome 2023-10-16 criteria provided, single submitter clinical testing

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