ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.465-17G>A

gnomAD frequency: 0.00001  dbSNP: rs761361803
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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 RCV000584108 SCV000691511 likely benign Hereditary cancer-predisposing syndrome 2016-11-22 criteria provided, single submitter clinical testing
GeneDx RCV001692215 SCV001913250 benign not provided 2015-09-16 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001809683 SCV002057411 likely benign Peutz-Jeghers syndrome 2021-07-15 criteria provided, single submitter clinical testing
Invitae RCV001809683 SCV002238152 likely benign Peutz-Jeghers syndrome 2024-01-15 criteria provided, single submitter clinical testing

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