ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.290+21_290+26dup

dbSNP: rs1555735086
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000663312 SCV000786575 likely benign Peutz-Jeghers syndrome 2018-05-29 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001177940 SCV001342256 likely benign Hereditary cancer-predisposing syndrome 2019-04-02 criteria provided, single submitter clinical testing
Invitae RCV000663312 SCV002437929 likely benign Peutz-Jeghers syndrome 2023-11-28 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002465747 SCV002761016 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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