ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.863-8C>T

gnomAD frequency: 0.00001  dbSNP: rs1224729035
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001176140 SCV001340019 uncertain significance Hereditary cancer-predisposing syndrome 2018-11-02 criteria provided, single submitter clinical testing
Invitae RCV001478697 SCV001682972 likely benign Peutz-Jeghers syndrome 2023-06-07 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001478697 SCV002057289 likely benign Peutz-Jeghers syndrome 2021-07-15 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV001176140 SCV002526953 uncertain significance Hereditary cancer-predisposing syndrome 2021-04-20 criteria provided, single submitter curation

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