ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.858G>A (p.Leu286=)

gnomAD frequency: 0.00001  dbSNP: rs770916046
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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 RCV000775658 SCV000910051 likely benign Hereditary cancer-predisposing syndrome 2018-02-06 criteria provided, single submitter clinical testing
Invitae RCV001495882 SCV001700572 likely benign Peutz-Jeghers syndrome 2019-03-20 criteria provided, single submitter clinical testing

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