ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.1108+12G>C

dbSNP: rs1057521545
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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 RCV000773219 SCV000906818 likely benign Hereditary cancer-predisposing syndrome 2016-10-12 criteria provided, single submitter clinical testing
Invitae RCV002067263 SCV002419180 likely benign Peutz-Jeghers syndrome 2024-01-15 criteria provided, single submitter clinical testing

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