ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.1109-8C>T

gnomAD frequency: 0.00001  dbSNP: rs1373424237
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000584482 SCV000691474 likely benign Hereditary cancer-predisposing syndrome 2016-08-05 criteria provided, single submitter clinical testing
Invitae RCV002061946 SCV002382529 likely benign Peutz-Jeghers syndrome 2024-01-18 criteria provided, single submitter clinical testing

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