ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.81C>T (p.His27=)

dbSNP: rs2080670824
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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 RCV001189261 SCV001356517 likely benign Hereditary cancer-predisposing syndrome 2019-02-08 criteria provided, single submitter clinical testing
Invitae RCV001426283 SCV001628933 likely benign Peutz-Jeghers syndrome 2023-01-24 criteria provided, single submitter clinical testing

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