ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.1109-20A>G

dbSNP: rs2145435720
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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 RCV003618130 SCV004376557 likely benign Peutz-Jeghers syndrome 2023-11-23 criteria provided, single submitter clinical testing

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