ClinVar Miner

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

dbSNP: rs1555737439
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Total submissions: 3
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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
Labcorp Genetics (formerly Invitae), Labcorp RCV002529284 SCV002944290 likely benign Peutz-Jeghers syndrome 2025-01-23 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005357768 SCV005915897 likely benign Peutz-Jeghers syndrome; Familial pancreatic carcinoma 2022-01-11 criteria provided, single submitter clinical testing

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