ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.450G>A (p.Val150=)

dbSNP: rs1555737821
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000548594 SCV000629115 likely benign Peutz-Jeghers syndrome 2024-02-12 criteria provided, single submitter clinical testing

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