ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.39G>C (p.Thr13=)

dbSNP: rs765330434
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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 RCV001463473 SCV001667417 likely benign Peutz-Jeghers syndrome 2022-05-11 criteria provided, single submitter clinical testing

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