ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.465-17GT[2]

dbSNP: rs749644491
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000663076 SCV000786150 likely benign Peutz-Jeghers syndrome 2018-03-08 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000771626 SCV000904234 likely benign Hereditary cancer-predisposing syndrome 2017-11-21 criteria provided, single submitter clinical testing
GeneDx RCV001692256 SCV001906586 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Invitae RCV000663076 SCV002445130 likely benign Peutz-Jeghers syndrome 2024-01-31 criteria provided, single submitter clinical testing

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